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510k Database
Manufacturers
US
Mmi, Inc.
Medical Device Manufacturer
·
US , Southfield , MI
Mmi, Inc. - FDA 510(k) Cleared Devices
3 submissions
·
3 cleared
·
Since 1984
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mmi, Inc.
Gastroenterology & Urology
✕
2
devices
1-2 of 2
Filters
Cleared
Dec 18, 1991
DUAL FLEX NON-LATEX
K905026
·
FGD
Gastroenterology & Urology
·
406d
Cleared
Aug 08, 1984
G.I. CLEANSING KIT
K842130
·
FCE
Gastroenterology & Urology
·
70d
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3
Gastroenterology & Urology
2
Obstetrics & Gynecology
1