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

DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS)

K Number: K902441 · Decision Aug 23, 1990
Classifications
1
FEI Numbers
329
Registration Numbers
330
Same Product Code
61
Applicant Total
13
Review Days
83

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Basic Information

Device Name
DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS)
K Number
K902441
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Applicant
Currie Medical Specialties, Inc.
Date Received
June 1, 1990
Decision Date
August 23, 1990
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

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K112311 ALP 501 RB PUMP SYSTEM
K874760 CK 4900 SERIES, GOWN AND TOWEL PAK
K872395 CK 1600 SERIES, TOWELS
K871737 CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTOR
K864816 CK 5000 SERIES, ACE BANDAGE/ESMARK BANDAGE
K864697 CK 6000 SERIES, TOWELS
K834558 CK10000 SERIES POUCH & BAGS ETC.
Search all 13 clearances from Currie Medical Specialties, Inc. →