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

FEM CATH (URETHRAL CATHETER)

K Number: K761144 · Decision Dec 6, 1976
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
92
Review Days
10

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Basic Information

Device Name
FEM CATH (URETHRAL CATHETER)
K Number
K761144
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Mallinckrodt Critical Care
Date Received
November 26, 1976
Decision Date
December 6, 1976
Product Code
KOD
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KOD Catheter, Urological

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Other Clearances by Mallinckrodt Critical Care

K Number Device Name
K880343 BURNEY GALLBLADDER CATHETER KIT
K874605 HI-LO TEMP(R) MYOCARDIAL TEMPERATURE SENSOR
K874514 HI-LO TEMP(R) GENERAL PURPOSE TEMPERATURE PROBE
K874568 HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR
K874404 HI-LO TEMP(R) SKIN TEMPERATURE SENSOR
K873461 LASER-FLEX(TM) TRACHEAL TUBE (CUFFED)
K873833 THERMOCOUPLE ADAPTER
K873004 GUIDING CATHETER
K871204 CUFFED TRACHEAL TUBE (MULTIPLE)
K862666 UNCUFFED LASER RESISTEANT TRACHEAL TUBE(TENTATIVE)
Search all 92 clearances from Mallinckrodt Critical Care →