ClearanceBrief
Company ยท US

Medical Marketing Group

FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 1991. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KNXCollector, Urine, (And Accessories) For Indwelling Catheter4
BYXTubing, Pressure And Accessories1
BYZTrap, Sterile Specimen1
FCMTray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)1
GAZTubing, Noninvasive1
GBMCatheter, Urethral1
KNYAccessories, Catheter, G-U1
KODCatheter, Urological1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 2, 1991K910022MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT
Medical Marketing Group
FCM
Feb 17, 1989K884819O'NEIL URINARY CATHETER INTRODUCER
Medical Marketing Group
KNY
Jan 27, 1988K874682MMG CATHETER PLUG W/DRAINAGE TUBE COVER
Medical Marketing Group
KOD
Aug 25, 1987K871999MMG URO-SELF CATHETER
Medical Marketing Group
GBM
Oct 27, 1986K863912THE MMG 5 IN 1 CONNECTOR
Medical Marketing Group
BYX
Mar 30, 1984K840838MMG CONNECTIVE TUBING
Medical Marketing Group
GAZ
May 24, 1982K821168DISPOSABLE URINARY LEGBAG W/STRAP
Medical Marketing Group
KNX
Jun 12, 1981K811469MMG URINARY DRAINAGE TUBING
Medical Marketing Group
KNX
May 30, 1980K800694MMG DISPOSABLE URINARY LEG BAG
Medical Marketing Group
KNX
Oct 2, 1979K791847ASPRI-LUKE
Medical Marketing Group
BYZ
Mar 6, 1979K790279CATHETER, MMG LATEX EXTERNAL
Medical Marketing Group
KNX

Latest recalls

DateFirm and productCodeLinked 510(k)
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