NUMOBAG— 510(k) K981949

Substantially Equivalent

Numotech, Inc.

FDA 510(k) clearance K981949 for NUMOBAG, Substantially Equivalent on 1999-02-03. Applicant: Numotech, Inc.. Device class: 2.

Clearance details

Applicant: Numotech, Inc.
Product code: Code KPJ
Device class: Class 2
Regulation: 21 CFR 878.5650
Advisory panel: General, Plastic Surgery
Date received: 1998-06-03
Decision date: 1999-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodland Hills, CA, US

Download summary PDF View on FDA.gov ↗

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