ACU-CURETTE— 510(k) K891334

Substantially Equivalent

Acuderm, Inc.

FDA 510(k) clearance K891334 for ACU-CURETTE, Substantially Equivalent on 1989-04-11. Applicant: Acuderm, Inc.. Device class: 1.

Clearance details

Applicant: Acuderm, Inc.
Product code: Code FZS
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1989-03-10
Decision date: 1989-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ft. Lauderdale, FL, US

Download summary PDF View on FDA.gov ↗

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K890366 — ADENOID CURETTE1989-02-03

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