STUART LEE CLIP— 510(k) K881741

Substantially Equivalent

Stuart-Lee, Inc.

FDA 510(k) clearance K881741 for STUART LEE CLIP, Substantially Equivalent on 1988-06-03. Applicant: Stuart-Lee, Inc.. Device class: 1.

Clearance details

Applicant: Stuart-Lee, Inc.
Product code: Code GDJ
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1988-04-22
Decision date: 1988-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waterford, CT, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.