FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

REPROCESSED TROCARS

K Number: K033591 · Decision Jun 3, 2005
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
2
Applicant Total
14
Review Days
568

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Basic Information

Device Name
REPROCESSED TROCARS
K Number
K033591
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4420
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clearmedical, Inc.
Date Received
November 13, 2003
Decision Date
June 3, 2005
Product Code
KBG
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
KBG Trocar, Sinus

Similar 510(k) Clearances

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

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Other Clearances by Clearmedical, Inc.

K Number Device Name
K033578 REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS
K033579 REPROCESSED MULTIPLE CLIP APPLIERS
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. →