Cavitron Corp. - FDA 510(k) Cleared Devices
32
Total
32
Cleared
0
Denied
Cavitron Corp. has 32 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 32 cleared submissions from 1976 to 1981.
Browse the FDA 510(k) cleared devices submitted by Cavitron Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cavitron Corp.
32 devices
Cleared
Jul 28, 1981
THE PLACER
Dental
53d
Cleared
Feb 13, 1981
MINOR SURGERY LIGHT
General & Plastic Surgery
18d
Cleared
Dec 17, 1980
SPIROMETRIC COMPUTER #SC-10
Anesthesiology
28d
Cleared
Nov 18, 1980
CAVITRON ULTRASONIC SURG. ASPIR. CUSA
General & Plastic Surgery
126d
Cleared
Sep 16, 1980
SLIT LAMP ATTACHMENT
Ophthalmic
41d
Cleared
May 28, 1980
MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA
Anesthesiology
41d
Cleared
Apr 29, 1980
AUTO-FIELD D AUTOMATED VISUAL DETECTOR
Ophthalmic
28d
Cleared
Sep 19, 1979
MODEL G-61 ULTRASONIC DENTAL UNIT
Dental
33d
Cleared
Aug 22, 1979
MODEL 6500 EXTRACTION IRRIGATION SYS
Obstetrics & Gynecology
43d
Cleared
Jan 17, 1979
LASER, CO2 SURGICAL
Obstetrics & Gynecology
41d
Cleared
Dec 28, 1978
LASER, PHOTOCOAGULATION
Ophthalmic
15d
Cleared
Sep 14, 1978
AUTO-FIELD II OPHTHALMIC FIELD SCANNER
Ophthalmic
20d