Sharplan Industries, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Sharplan Industries, Inc. has 4 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 4 cleared submissions from 1986 to 1986. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Sharplan Industries, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sharplan Industries, Inc.
4 devices
Cleared
Oct 28, 1986
MODEL 2100 ND:YAG SURGICAL LASER NEUROSURGICAL IND
General & Plastic Surgery
224d
Cleared
Jun 17, 1986
MODEL 2100 ND:YAG SURGICAL LASER GASTROINTESTINAL
Gastroenterology & Urology
91d
Cleared
May 02, 1986
MODEL 2100 ND:YAG SURGICAL LASER UROLOGICAL INDICA
Gastroenterology & Urology
45d
Cleared
Apr 23, 1986
MODEL 2100 ND:YAG SURGICAL LASER PULMONARY INDICAT
Anesthesiology
36d