THE DE SOUTTER M193 REAMER— 510(k) K930784

Name: FDA 510(k) clearance K930784
Creator: U.S. Food and Drug Administration
Published: 1993-10-27

Substantially Equivalent

De Soutter Medical, Ltd.

FDA 510(k) clearance K930784 for THE DE SOUTTER M193 REAMER, Substantially Equivalent on 1993-10-27. Applicant: De Soutter Medical, Ltd.. Device class: 1.

Clearance details

Applicant: De Soutter Medical, Ltd.
Product code: Code HSZ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1993-02-16
Decision date: 1993-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kings Langley Herts, GB

Download summary PDF View on FDA.gov ↗

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