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

REPROCESSED DISPOSABLE TROCARS

K Number: K022743 · Decision Oct 9, 2002
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
0
Applicant Total
5
Review Days
51

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Basic Information

Device Name
REPROCESSED DISPOSABLE TROCARS
K Number
K022743
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
Medical Device Services
Date Received
August 19, 2002
Decision Date
October 9, 2002
Product Code
KAB
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
KAB Trocar, Laryngeal

Other Clearances by Medical Device Services

K Number Device Name
K022753 REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS
K022751 REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS
K022748 REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS
K022744 REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS