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

TROCAR CATHETER

K Number: K913678 · Decision Dec 16, 1991
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
5
Applicant Total
31
Review Days
119

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Basic Information

Device Name
TROCAR CATHETER
K Number
K913678
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4100
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medovations, Inc.
Date Received
August 19, 1991
Decision Date
December 16, 1991
Product Code
KGY
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
KGY Bag, Intestine

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Other Clearances by Medovations, Inc.

K Number Device Name
K142068 BULLDOG BIOPSY VALVE, OLYMPUS AND FUJINON;PENTAX COMPATIBLE;DISPOSABLE RRIGATING ADAPTOR, STERILE AND NON-STERILE
K002363 MEDOVATIONS ESOPHAGEAL DILATOR
K972119 MALONEY BOUGE (1210-XX)/HURST BOUGIE (1212-XX)
K924646 OVER THE GUIDEWIRE DILATATION SYSTEM
K905478 YANKAUER SUCTION DEVICE
K874309 URETHAL CATHETER
K864963 STOMACH EVACULATOR - EWALD STYLE
K864962 OBERTO MOUTH PROP
K864964 5 - IN - 1 CONNECTOR
K854616 ENTERAL FEEDING BAG
Search all 31 clearances from Medovations, Inc. →