FDA 510(k) FDA class 1 Unknown 🇺🇸 United States

STERILE SURGICAL INSTRUMENT TRAYS

K Number: K925215 · Decision Jun 1, 1993
Classifications
1
FEI Numbers
329
Registration Numbers
330
Same Product Code
61
Applicant Total
5
Review Days
228

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Basic Information

Device Name
STERILE SURGICAL INSTRUMENT TRAYS
K Number
K925215
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Statement
Applicant
American Healthcare Supply Co., Inc.
Date Received
October 16, 1992
Decision Date
June 1, 1993
Product Code
KDD
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
KDD Kit, Surgical Instrument, Disposable

Similar 510(k) Clearances

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

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Other Clearances by American Healthcare Supply Co., Inc.

K Number Device Name
K925214 SHAVE PREP TRAYS (NON-STERILE)
K925216 STERILE SKIN SCRUB TRAYS
K924835 VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560
K924834 PREMIERE STERILE SUTURE REMOVAL KIT(HC-50-54957)