CARESTREAM MEDICAL

FDA Device Registration & Listing · Sanford, FL, US · Registration 3010396502

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
3010396502
FEI Number
3010396502
Entity Name
CARESTREAM MEDICAL
City/State/Country
Sanford, FL, US
Establishment Address
1201 Upsala Rd, Sanford, FL 32771, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
CAREstream Medical LTD (Owner Number: 10044901)
Owner / Operator Contact Address
443 Palm Crest Lane, Lake Mary, FL 32746, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K110930
PMA Number
N/A

All Registered Proprietary Names

Passive waste gas scavenger model 14600 Pro-Nox Pro-Vac Blower Active Waste Gas Scavenger

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CBN Apparatus, Gas-Scavenging Anesthesiology Class 2 868.5430 2024-05-15
BZR Mixer, Breathing Gases, Anesthesia Inhalation Anesthesiology Class 2 868.5330 2023-04-20
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered General Hospital Class 2 880.6740 2025-08-29
CBN Apparatus, Gas-Scavenging Anesthesiology Class 2 868.5430 2024-05-15

Official Correspondent

Scott Petrunick

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CAREstream Medical LTD
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010396502. Last updated year: 2026. Please use registration number 3010396502 when referencing this establishment in official correspondence.
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