KELMAN DIPSTICK— 510(k) K792383

Name: FDA 510(k) clearance K792383
Creator: U.S. Food and Drug Administration
Published: 1979-12-11

Substantially Equivalent

V. Mueller O.V. Baxter Healthcare Corp.

FDA 510(k) clearance K792383 for KELMAN DIPSTICK, Substantially Equivalent on 1979-12-11. Applicant: V. Mueller O.V. Baxter Healthcare Corp.. Device class: 1.

Clearance details

Applicant: V. Mueller O.V. Baxter Healthcare Corp.
Product code: Code HOE
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1979-11-26
Decision date: 1979-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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