Full Spectrum, Inc. is one of 25897 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Full Spectrum, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FSI LAPAROSCOPIC PROBE FOR ALL FSI ULE-OVERCLAD FF201 FIBERS, (FSI) LAPAROSCOPIC PROBE FOR ALL FSI ULE FF101 FIBERS. MODEL FSI FF101-LP-XXX, WHERE XXX = FIBER DIAMETERS 100, 200, 400, FULL SPECTRUM ULE-OVERCLAD FIBER: MODEL 201
3
Total
3
Cleared
0
Denied
Full Spectrum, Inc. has 3 FDA 510(k) cleared medical devices. Based in Ames, US.
Historical record: 3 cleared submissions from 1996 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Full Spectrum, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Full Spectrum, Inc.
3 devices
Cleared
Apr 24, 1997
FSI LAPAROSCOPIC PROBE FOR ALL FSI ULE-OVERCLAD FF201 FIBERS
General & Plastic Surgery
202d
Cleared
Apr 24, 1997
(FSI) LAPAROSCOPIC PROBE FOR ALL FSI ULE FF101 FIBERS. MODEL FSI...
General & Plastic Surgery
202d
Cleared
Mar 01, 1996
FULL SPECTRUM ULE-OVERCLAD FIBER: MODEL 201
General & Plastic Surgery
65d