Precise Optics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - Precise Optics
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