SECHRIST AIR-OXYGEN MIXER, 3500/3500HL SERIES— 510(k) K992503

Name: FDA 510(k) clearance K992503
Creator: U.S. Food and Drug Administration
Published: 1999-08-10

Substantially Equivalent

Sechrist Industries, Inc.

FDA 510(k) clearance K992503 for SECHRIST AIR-OXYGEN MIXER, 3500/3500HL SERIES, Substantially Equivalent on 1999-08-10. Applicant: Sechrist Industries, Inc.. Device class: 2.

Clearance details

Applicant: Sechrist Industries, Inc.
Product code: Code BZR
Device class: Class 2
Regulation: 21 CFR 868.5330
Advisory panel: Anesthesiology
Date received: 1999-07-27
Decision date: 1999-08-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Anaheim, CA, US

Download summary PDF View on FDA.gov ↗

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