SERIES 25 SLIMLINE CRYO PROBES— 510(k) K854422

Name: FDA 510(k) clearance K854422
Creator: U.S. Food and Drug Administration
Published: 1985-12-30

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K854422 for SERIES 25 SLIMLINE CRYO PROBES, Substantially Equivalent on 1985-12-30. Applicant: Keeler Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HQA
Device class: Class 2
Regulation: 21 CFR 886.4170
Advisory panel: Ophthalmic
Date received: 1985-11-04
Decision date: 1985-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

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