MAHE INSTRUMENTS— 510(k) K942823

Substantially Equivalent

Mahe Intl., Inc.

FDA 510(k) clearance K942823 for MAHE INSTRUMENTS, Substantially Equivalent on 1994-12-05. Applicant: Mahe Intl., Inc.. Device class: 2.

Clearance details

Applicant: Mahe Intl., Inc.
Product code: Code DWG
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1994-06-14
Decision date: 1994-12-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nashville, TN, US

Download summary PDF View on FDA.gov ↗

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