Sharplan Lasers, Inc. - FDA 510(k) Cleared Devices
78
Total
78
Cleared
0
Denied
Sharplan Lasers, Inc. has 78 FDA 510(k) cleared general & plastic surgery devices. Based in Allendale, US.
Historical record: 78 cleared submissions from 1986 to 1997.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
78 devices
Cleared
Dec 04, 1997
SHARPLAN EPITOUCH ALEXANDRITE LASER SYSTEM (5000)
General & Plastic Surgery
90d
Cleared
Aug 27, 1997
SHARPLAN EPITOUCH RUBY LASER SYSTEM
General & Plastic Surgery
84d
Cleared
Aug 18, 1997
SHARPLAN EPITOUCH ALEXANDRITE LASER SYSTEM (5000)
General & Plastic Surgery
90d
Cleared
Jul 23, 1997
SHARPLAN ERBIUM: YAG LASER (4020)
General & Plastic Surgery
79d
Cleared
Jul 18, 1997
SHARPLAN CO2 SURGICAL LASER SYSTEM
General & Plastic Surgery
67d
Cleared
Mar 07, 1997
SHARPLAN RUBY LASER SYSTEM
General & Plastic Surgery
256d
Cleared
Nov 05, 1996
SHARPLAN MODELS 20C, 30C, AND 40C CO2 LASERS
General & Plastic Surgery
78d
Cleared
Nov 01, 1996
SHARPLAN LASERS, INC. SILKTOUCH CO2 FLASH SCANNER
General & Plastic Surgery
165d
Cleared
Aug 21, 1996
SHARPLAN LASERS, INC. AF ACUSPOT MICROMANIPULATOR (713)
General & Plastic Surgery
21d
Cleared
Jun 18, 1996
SHARPLAN LASERS, INC. RUBY LASER SYSTEM
General & Plastic Surgery
76d
Cleared
May 10, 1996
SHARPLAN LASERS, INC. SILKTOUCH XJ SCANNER
General & Plastic Surgery
71d
Cleared
Apr 29, 1996
SHARPLAN ULTRA LAPAROSCOPIC HANDPIECE
General & Plastic Surgery
118d
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