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

DISPOSABLE COUPLING ADAPTOR

K Number: K801261 · Decision Jun 9, 1980
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
61
Applicant Total
17
Review Days
12

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DISPOSABLE COUPLING ADAPTOR
K Number
K801261
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5860
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Intec Medical, Inc.
Date Received
May 28, 1980
Decision Date
June 9, 1980
Product Code
BYX
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BYX Tubing, Pressure And Accessories

Similar 510(k) Clearances

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

View all

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
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
Search all 17 clearances from Intec Medical, Inc. →