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

CATHETER, EXTERNAL MALE NURSING CARE

K Number: K781780 · Decision Dec 7, 1978
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
36
Review Days
50

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Basic Information

Device Name
CATHETER, EXTERNAL MALE NURSING CARE
K Number
K781780
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Medi-Tech, Inc.
Date Received
October 18, 1978
Decision Date
December 7, 1978
Product Code
KNX
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
KNX Collector, Urine, (And Accessories) For Indwelling Catheter

Similar 510(k) Clearances

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Other Clearances by Medi-Tech, Inc.

K Number Device Name
K954457 MEDI-TECH EDDY INTRAVASCULAR INFUSION CATHETER
K952345 MEDI-TECH PLATFORM GUIDE CATHETER
K952056 IMMUNOASSAY DRUGS OF ABUSE CONTROLS
K945289 DOA - IMMUNOASSAY CUT-OFF CALIBRATOR
K942551 THERAPEUTIC DRUG MONITORING CONTROL, ASSAYED
K943290 BILIRUBIN PLUS/PEDIATRIC CONTROLS
K922990 HEMODIALYSIS BATH
K942552 THERAPEUTIC DRUG MONITORING CONTROL, UNASSAYED
K904073 COAGULATION REFERENCE PLASMA, ABNORMAL
K895819 MODIFIED LABELING TO THE SPAND-GEL GRANULATED GEL
Search all 36 clearances from Medi-Tech, Inc. →