PNEUMATIC DEMAND OXYGEN CONSERVER (PDOC)— 510(k) K990678

Name: FDA 510(k) clearance K990678
Creator: U.S. Food and Drug Administration
Published: 1999-05-07

Substantially Equivalent

Salter Labs

FDA 510(k) clearance K990678 for PNEUMATIC DEMAND OXYGEN CONSERVER (PDOC), Substantially Equivalent on 1999-05-07. Applicant: Salter Labs. Device class: 2.

Clearance details

Applicant: Salter Labs
Product code: Code NFB
Device class: Class 2
Regulation: 21 CFR 868.5905
Advisory panel: Anesthesiology
Date received: 1999-03-02
Decision date: 1999-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arvin, CA, US

Download summary PDF View on FDA.gov ↗

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