SURGICAL CURETTE— 510(k) K932493

Substantially Equivalent

Whitney Products, Inc.

FDA 510(k) clearance K932493 for SURGICAL CURETTE, Substantially Equivalent on 1994-01-07. Applicant: Whitney Products, Inc.. Device class: 1.

Clearance details

Applicant: Whitney Products, Inc.
Product code: Code FZS
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1993-05-24
Decision date: 1994-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glenview, IL, US

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