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

BAHADIR STERILIZATION TRAYS

K Number: K112090 · Decision Jun 7, 2012
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
3
Review Days
322

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Basic Information

Device Name
BAHADIR STERILIZATION TRAYS
K Number
K112090
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bahadir USA Corp.
Date Received
July 21, 2011
Decision Date
June 7, 2012
Product Code
KCT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Similar 510(k) Clearances

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

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Other Clearances by Bahadir USA Corp.

K Number Device Name
K131407 BAHADIR STERILIZATION TRAYS
K102146 BAHADIR STERILIZATION TRAYS