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

REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS

K Number: K033578 · Decision Jul 11, 2005
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
2
Applicant Total
14
Review Days
606

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Basic Information

Device Name
REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS
K Number
K033578
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4750
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clearmedical, Inc.
Date Received
November 13, 2003
Decision Date
July 11, 2005
Product Code
NLL
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
NLL Staple, Implantable, Reprocessed

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Other Clearances by Clearmedical, Inc.

K Number Device Name
K033579 REPROCESSED MULTIPLE CLIP APPLIERS
K033591 REPROCESSED TROCARS
K033592 REPROCESSED SURGICAL SCISSORS AND GRASPERS
K033593 REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS
K031416 CLEARMEDICAL/CRITIKON BLOOD PRESSURE CUFF; CLEARMEDICAL/WELCH ALLYN BLOOD PRESSURE CUFF
K012600 CLEARMEDICAL/NELLCOR OXISENSOR II, ADULT, MODEL D-25/D-25L
K012622 CLEARMEDICAL/NELLCOR OXISENSOR II, PEDIATRIC, MODEL D-20
K012609 CLEARMEDICAL/NELLCOR OXISENSOR II, NEONATAL/ADULT, MODEL N-25
K012601 CLEARMEDICAL/AIRCAST VENAFLOW CALF CUFF, CLEARMEDICAL AIRCAST XL VENAFLOW CALF CUFF, CLEARMEDICAL/AIRCAST VENAFLOW THIGH
K012621 CLEARMEDICAL/HENTLEIGH DEEP VEIN THROMBOSIS (DVT) GARMENT
Search all 14 clearances from Clearmedical, Inc. →