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

PERCUTANEOUS CATHETER INTRODUCER KIT

K Number: K903906 · Decision Sep 26, 1990
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
17
Review Days
34

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Basic Information

Device Name
PERCUTANEOUS CATHETER INTRODUCER KIT
K Number
K903906
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Intec Medical, Inc.
Date Received
August 23, 1990
Decision Date
September 26, 1990
Product Code
DYB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DYB Introducer, Catheter

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Other Clearances by Intec Medical, Inc.

K Number Device Name
K911840 INTERFLO MEDICAL MODEL PA3-H CCO/PAC CATHETER
K903217 TAPERED TIP THE GUIDER CORONARY GUIDING CATHETER
K903216 THE GUIDER CORONARY GUIDING CATHETER
K900710 INTERFLO MEDICAL MODEL F-1 THERMODILUTION CATHETER
K903840 GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY
K900998 INTERVENTIONAL MEDICAL Y ADAPTER W/ADJUST. VALVE
K901247 TRI ADAPTER W/ADJUSTABLE HEMOSTASIS VALVES
K894925 AMCATH URETERAL DILATORS MODELS 7100,7110,7120
K860941 DISPOSABLE HEATED WIRE LOOPS 48 AND 72
K823271 DISPOSABLE ADULT VO. VENTILATOR CIRCUIT
Search all 17 clearances from Intec Medical, Inc. →