KEELER CRYO MASTER & PROBES— 510(k) K992954

Name: FDA 510(k) clearance K992954
Creator: U.S. Food and Drug Administration
Published: 1999-12-21

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K992954 for KEELER CRYO MASTER & PROBES, Substantially Equivalent on 1999-12-21. Applicant: Keeler Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HRN
Device class: Class 2
Regulation: 21 CFR 886.4170
Advisory panel: Ophthalmic
Date received: 1999-09-01
Decision date: 1999-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

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