FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ACU-DISPO-CE(TM)

K Number: K933265 · Decision Mar 7, 1994
Classifications
1
FEI Numbers
840
Registration Numbers
840
Same Product Code
43
Applicant Total
13
Review Days
244

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Basic Information

Device Name
ACU-DISPO-CE(TM)
K Number
K933265
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Acuderm, Inc.
Date Received
July 6, 1993
Decision Date
March 7, 1994
Product Code
MDM
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
MDM Instrument, Manual, Surgical, General Use

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MDM), ordered by most recent decision date.

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Other Clearances by Acuderm, Inc.

K Number Device Name
K933516 ACU-E PUNCH
K933137 ACU-SUTURE KIT
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. →