Cavitron Corp. - FDA 510(k) Cleared Devices
32
Total
32
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cavitron Corp. Ophthalmic ✕
6 devices
Cleared
Sep 16, 1980
SLIT LAMP ATTACHMENT
Ophthalmic
41d
Cleared
Apr 29, 1980
AUTO-FIELD D AUTOMATED VISUAL DETECTOR
Ophthalmic
28d
Cleared
Dec 28, 1978
LASER, PHOTOCOAGULATION
Ophthalmic
15d
Cleared
Sep 14, 1978
AUTO-FIELD II OPHTHALMIC FIELD SCANNER
Ophthalmic
20d
Cleared
Sep 07, 1978
AUTOREFRACTOR, SUBJECTIVE
Ophthalmic
83d
Cleared
May 09, 1978
PHOTOCOAGULATOR LASER
Ophthalmic
69d