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

MMG URINARY DRAINAGE TUBING

K Number: K811469 · Decision Jun 12, 1981
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
11
Review Days
17

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Basic Information

Device Name
MMG URINARY DRAINAGE TUBING
K Number
K811469
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Medical Marketing Group
Date Received
May 26, 1981
Decision Date
June 12, 1981
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

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

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Other Clearances by Medical Marketing Group

K Number Device Name
K910022 MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT
K884819 O'NEIL URINARY CATHETER INTRODUCER
K874682 MMG CATHETER PLUG W/DRAINAGE TUBE COVER
K871999 MMG URO-SELF CATHETER
K863912 THE MMG 5 IN 1 CONNECTOR
K840838 MMG CONNECTIVE TUBING
K821168 DISPOSABLE URINARY LEGBAG W/STRAP
K800694 MMG DISPOSABLE URINARY LEG BAG
K791847 ASPRI-LUKE
K790279 CATHETER, MMG LATEX EXTERNAL
Search all 11 clearances from Medical Marketing Group →