Atlas FDA

ACU-E PUNCH

FDA 510(k) clearance K933516 · decided 1994-03-24

Clearance details

K-number
K933516
Device name
ACU-E PUNCH
Applicant
Acuderm, Inc.
Decision
Substantially Equivalent
Date received
1993-07-20
Decision date
1994-03-24
Days to decision
247 days
Clearance type
Traditional
Product code
LRY
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Ft. Lauderdale, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ELLIPSE PUNCH (K904869)Kramer Const1991-03-06
LIPOGEN RHEUMELISA DSDNA ASSAY (K902636)Lipogen, Inc.1990-06-28
BIOPSY PUNCH (K896303)Premier Medical1990-02-13
PIN PUNCH (K874356)Med-Tool, Inc.1987-11-23
TAPERED PUNCH (K874357)Med-Tool, Inc.1987-11-23
NAIL SET (K872388)Med-Tool, Inc.1987-07-23

Recalls involving this device

No recalls on record reference this clearance.