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

TAPERED TIP THE GUIDER CORONARY GUIDING CATHETER

K Number: K903217 · Decision Oct 19, 1990
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
17
Review Days
88

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Basic Information

Device Name
TAPERED TIP THE GUIDER CORONARY GUIDING CATHETER
K Number
K903217
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Intec Medical, Inc.
Date Received
July 23, 1990
Decision Date
October 19, 1990
Product Code
DQY
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
DQY Catheter, Percutaneous

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Other Clearances by Intec Medical, Inc.

K Number Device Name
K911840 INTERFLO MEDICAL MODEL PA3-H CCO/PAC CATHETER
K903216 THE GUIDER CORONARY GUIDING CATHETER
K900710 INTERFLO MEDICAL MODEL F-1 THERMODILUTION CATHETER
K903840 GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY
K903906 PERCUTANEOUS CATHETER INTRODUCER KIT
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. →