BOUGIE, FILIFORM, JACKSON— 510(k) K770959

Name: FDA 510(k) clearance K770959
Creator: U.S. Food and Drug Administration
Published: 1977-06-14

Substantially Equivalent

V. Mueller O.V. Baxter Healthcare Corp.

FDA 510(k) clearance K770959 for BOUGIE, FILIFORM, JACKSON, Substantially Equivalent on 1977-06-14. Applicant: V. Mueller O.V. Baxter Healthcare Corp.. Device class: 1.

Clearance details

Applicant: V. Mueller O.V. Baxter Healthcare Corp.
Product code: Code KBI
Device class: Class 1
Regulation: 21 CFR 874.4175
Advisory panel: Ear, Nose, Throat
Date received: 1977-05-27
Decision date: 1977-06-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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