Full Spectrum, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Full Spectrum, Inc. General & Plastic Surgery ✕
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