Precise Optics - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Precise Optics has 13 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 13 cleared submissions from 1979 to 2003. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Precise Optics Filter by specialty or product code using the sidebar.
13 devices
Cleared
Apr 07, 2003
PS 3000 DIGATAL PHOTOSPOT SYSTEM
Radiology
90d
Cleared
Mar 16, 1994
PHF20 20 MOBILE C-ARM IMAGE INTENSIFIER
Radiology
118d
Cleared
Jan 06, 1994
PRECISION INTRA-ORAL SCOPES
Dental
206d
Cleared
Jan 22, 1992
ENDOSCOPES
General & Plastic Surgery
140d
Cleared
Nov 27, 1991
P2020-8-0 BEAM-LIMITING DEVICE
Radiology
70d
Cleared
Jul 26, 1991
PRECISION OPTICS CORPORATION LAPAROSCOPE
General & Plastic Surgery
99d
Cleared
Oct 26, 1990
PRECISION OPTICS ENDOSCOPE ADAPTER
Gastroenterology & Urology
86d
Cleared
Oct 19, 1990
PRECISION OPTICS IMAGE BEAMSPLITTER (COUPLER)
Gastroenterology & Urology
79d
Cleared
Oct 19, 1990
PRECISION OPTICS IMAGE COUPLER
Gastroenterology & Urology
79d
Cleared
Mar 04, 1982
PI808 MOBILE C-ARM IMAGE INTENSIFIER
Radiology
41d
Cleared
Mar 04, 1982
P1808 MOBILE C-ARM IMAGE INTENSIFIER
Radiology
41d
Cleared
Jan 09, 1980
DENTIX DENTAL X-RAY UNIT
Radiology
54d
Cleared
Dec 20, 1979
P1806 MOBILE C-ARM IMAGE INTENSIFIER
Radiology
45d