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

MMG URO-SELF CATHETER

K Number: K871999 · Decision Aug 25, 1987
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
70
Applicant Total
11
Review Days
91

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Basic Information

Device Name
MMG URO-SELF CATHETER
K Number
K871999
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Medical Marketing Group
Date Received
May 26, 1987
Decision Date
August 25, 1987
Product Code
GBM
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
GBM Catheter, Urethral

Similar 510(k) Clearances

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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
K863912 THE MMG 5 IN 1 CONNECTOR
K840838 MMG CONNECTIVE TUBING
K821168 DISPOSABLE URINARY LEGBAG W/STRAP
K811469 MMG URINARY DRAINAGE TUBING
K800694 MMG DISPOSABLE URINARY LEG BAG
K791847 ASPRI-LUKE
K790279 CATHETER, MMG LATEX EXTERNAL
Search all 11 clearances from Medical Marketing Group →