Medical Device Manufacturer · US , Kentwood , MI

Inrad - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1998
11
Total
11
Cleared
0
Denied

FDA 510(k) Regulatory Record - Inrad General & Plastic Surgery ✕

4 devices
1-4 of 4
Cleared Jan 30, 2007
ULTRACLIP II WING AND ULTRACLIP II COIL
K063238 · NEU
General & Plastic Surgery · 96d
Cleared Sep 20, 2004
ULTRACLIP II US
K042341 · NEU
General & Plastic Surgery · 21d
Cleared Jun 03, 2004
ULTRACLIP II MR
K041201 · GDW
General & Plastic Surgery · 27d
Cleared Feb 04, 2000
ULTRACLIP TISSUE MARKER
K993785 · GDW
General & Plastic Surgery · 88d
Filters
Filter by Specialty
All11 Gastroenterology & Urology 6 General & Plastic Surgery 4 General Hospital 1