FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT

K Number: K910022 · Decision Apr 2, 1991
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
59
Applicant Total
11
Review Days
89

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Basic Information

Device Name
MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT
K Number
K910022
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Applicant
Medical Marketing Group
Date Received
January 3, 1991
Decision Date
April 2, 1991
Product Code
FCM
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
FCM Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)

Similar 510(k) Clearances

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

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Other Clearances by Medical Marketing Group

K Number Device Name
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
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 →