FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ACU-SUTURE KIT

K Number: K933137 · Decision Feb 22, 1994
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
109
Applicant Total
13
Review Days
239

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Basic Information

Device Name
ACU-SUTURE KIT
K Number
K933137
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Acuderm, Inc.
Date Received
June 28, 1993
Decision Date
February 22, 1994
Product Code
LRO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LRO General Surgery Tray

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Other Clearances by Acuderm, Inc.

K Number Device Name
K933516 ACU-E PUNCH
K933265 ACU-DISPO-CE(TM)
K930043 ACU-EVAC
K933866 ACU-HEMOSTATIC RING
K915000 ACU-GUARD
K891334 ACU-CURETTE
K874024 ACU-MICRO-NEEDLE
K854877 ACU-SYRINGE W/WO NEEDLES
K832582 MYCOSEL AGAR
K832583 SABOURAUD DEXTROSE AGAR
Search all 13 clearances from Acuderm, Inc. →