SOLSTICE XRAY RING MARKER PAD
May 1993
182d
Solstice Corp.
1
Total
1
Cleared
0
Denied
Solstice Corp. — FDA 510(k) Submissions
Solstice Corp. has submitted 1 FDA 510(k) premarket notifications since 1993, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, X-ray, Film Marking, Radiographic . Use the specialty filter in the sidebar to narrow results.
1 devices