SECHRIST INDUSTRIES, INC.

FDA Device Registration & Listing · Anaheim, CA, US · Registration 2020676

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
2020676
FEI Number
2020676
Entity Name
SECHRIST INDUSTRIES, INC.
City/State/Country
Anaheim, CA, US
Establishment Address
4225 E LA PALMA AVE, Anaheim, CA 92807, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SECHRIST INDUSTRIES, INC. (Owner Number: 2020676)
Owner / Operator Contact Address
4225 EAST LA PALMA AVE., --, Anaheim, CA 92807, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Sechrist 3200P/PR Monoplace Hyperbaric Chamber Sechrist 4100H/HR Monoplace Hyperbaric Chamber HBO Cable assembly, radiometer Sechrist 3300E/ER Monoplace Hyperbaric Chamber Hydraulic Gurney Electric (E-Gurney) Wheeled Stretcher EZ Load Hydraulic Gurney Patient Transport (Gurney) Stretcher Hyperbaric Electronic Records Organizer (H.E.R.O.) eHEAL Sechrist Hyperbaric Ventilator Model 500A HBO Demand Valve Assembly Sechrist 2800/R Monoplace Hyperbaric Chamber 3500 Series Air/Oxygen Mixer Sechrist 3600E/ER Monoplace Hyperbaric Chamber

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CBF Chamber, Hyperbaric Anesthesiology Class 2 868.5470 2007-12-13
CBF Chamber, Hyperbaric Anesthesiology Class 2 868.5470 2010-11-24
LKD Monitor, Carbon-Dioxide, Cutaneous Anesthesiology Class 2 868.2480 2008-03-07
CBF Chamber, Hyperbaric Anesthesiology Class 2 868.5470 2007-12-13
FPO Stretcher, Wheeled General Hospital Class 2 880.6910 2011-11-10
OUG Medical Device Data System General Hospital Class 1 880.6310 2011-11-10
CBK Ventilator, Continuous, Facility Use Anesthesiology Class 2 868.5895 2008-06-11
CBP Valve, Non-Rebreathing Anesthesiology Class 2 868.5870 2008-03-07
CBF Chamber, Hyperbaric Anesthesiology Class 2 868.5470 2007-12-13
BZR Mixer, Breathing Gases, Anesthesia Inhalation Anesthesiology Class 2 868.5330 2007-12-13
CBF Chamber, Hyperbaric Anesthesiology Class 2 868.5470 2007-12-13

Official Correspondent

Victor Arellano

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SECHRIST INDUSTRIES, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K051895 Datex-Ohmeda, Inc. GE DATEX-OHMEDA ENGSTROM CARESTATION 2005-09-27
K082966 Covidien, Formerly Nellcor Puritan Bennett, Inc. PB 540 VENTILATOR 2008-10-31
K945177 Eagle Health Supplies 4-O2 JR. (CPR MOUTH BARRIER) 1994-11-01

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0023-05 Stryker Medical 2
Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092.
Z-0008-2015 Respironics California Inc 2
Esprit V1000 and V200 Ventilators, Model No. V1000 and V200; and the 3rd Generation Power Supply Repair Part (RP)Kits Microprocessor-controlled, electrically powered mechanical ventilators intended for use by qualified medical personnel to provide continuous or intermittent ventilator support for adult, pediatric and neonatal patients as prescribed by a physician.
Z-0018-2011 Draeger Medical Systems, Inc. 2
Oxylog 3000, Emergency and Transport Ventilator; Catalog #2M86300; Drager Medical Inc., 3135 Quarry Road, Telford, PA 18969.
Z-0112-2015 Nellcor Puritan Bennett Inc. (dba Covidien LP) 2
Covidien Puritan Bennett 980 Ventilator, Rx ONLY. Suitable for service in a hospital (institutions) and intra-hospital transport to provide continuous positive pressure ventilator for Neonatal (NICU) through Adult patient populations.
Z-0180-2015 Nellcor Puritan Bennett Inc. (dba Covidien LP) 2
Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien LLC, USA. REF 980X1ENDIUU.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2020676. Last updated year: 2026. Please use registration number 2020676 when referencing this establishment in official correspondence.
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