CONVERSE ALTAR RETRACTOR— 510(k) K760851

Name: FDA 510(k) clearance K760851
Creator: U.S. Food and Drug Administration
Published: 1977-03-10

Substantially Equivalent

V. Mueller O.V. Baxter Healthcare Corp.

FDA 510(k) clearance K760851 for CONVERSE ALTAR RETRACTOR, Substantially Equivalent on 1977-03-10. Applicant: V. Mueller O.V. Baxter Healthcare Corp.. Device class: 1.

Clearance details

Applicant: V. Mueller O.V. Baxter Healthcare Corp.
Product code: Code KAL
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Date received: 1976-10-15
Decision date: 1977-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K770959 — BOUGIE, FILIFORM, JACKSON1977-06-14

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