BABYFLEX PATIENT CIRCUIT— 510(k) K874559

Name: FDA 510(k) clearance K874559
Creator: U.S. Food and Drug Administration
Published: 1987-12-21

Substantially Equivalent

Airoflex Medical, Inc.

FDA 510(k) clearance K874559 for BABYFLEX PATIENT CIRCUIT, Substantially Equivalent on 1987-12-21. Applicant: Airoflex Medical, Inc.. Device class: 1.

Clearance details

Applicant: Airoflex Medical, Inc.
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1987-11-04
Decision date: 1987-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Riverside, CA, US

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K952012 — PRIMA CUSTOM ANESTESIA CIRCUIT1995-05-22

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