STEINWAY MICRO-KERATO-TREPHINE— 510(k) K843646

Name: FDA 510(k) clearance K843646
Creator: U.S. Food and Drug Administration
Published: 1985-01-03

Substantially Equivalent

Steinway Instrument Co., Inc.

FDA 510(k) clearance K843646 for STEINWAY MICRO-KERATO-TREPHINE, Substantially Equivalent on 1985-01-03. Applicant: Steinway Instrument Co., Inc.. Device class: 1.

Clearance details

Applicant: Steinway Instrument Co., Inc.
Product code: Code HRH
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1984-09-17
Decision date: 1985-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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