MED SYSTEMS

FDA Device Registration & Listing · SAN DIEGO, CA, US · Registration 2022691

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
2022691
FEI Number
2022691
Entity Name
MED SYSTEMS
City/State/Country
SAN DIEGO, CA, US
Establishment Address
2631 ARIANE DR., SAN DIEGO, CA 92117, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MED SYSTEMS (Owner Number: 2022691)
Owner / Operator Contact Address
2631 ARIANE DR., --, San Diego, CA 92117, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K031876
PMA Number
N/A

All Registered Proprietary Names

FLUID FLOW MEDS SERIES 2100 MASK ELECTRO FLO PERCUSSOR

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GWZ Percussor Neurology Class 1 882.1700 1992-10-20
BSJ Mask, Gas, Anesthetic Anesthesiology Class 1 868.5550 1992-10-20
BYI Percussor, Powered-Electric Anesthesiology Class 2 868.5665 2006-10-26

Official Correspondent

SUSAN DAVIS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MED SYSTEMS
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2022691. Last updated year: 2026. Please use registration number 2022691 when referencing this establishment in official correspondence.
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