Medical Device Manufacturer · US , Mchenry , IL

Cavitron Corp. - FDA 510(k) Cleared Devices

32 submissions · 32 cleared · Since 1976

Total

Cleared

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.

Cavitron Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cavitron Corp.

32 devices

1-12 of 32

General & Plastic Surgery · 18d

Cleared Dec 17, 1980

SPIROMETRIC COMPUTER #SC-10

K802928 · BZC

Anesthesiology · 28d

Cleared Nov 18, 1980

CAVITRON ULTRASONIC SURG. ASPIR. CUSA

K801623 · LFL

General & Plastic Surgery · 126d

MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA

K800869 · CCK

Anesthesiology · 41d

Cleared Apr 29, 1980

AUTO-FIELD D AUTOMATED VISUAL DETECTOR

K800722 · HPT

Ophthalmic · 28d

Cleared Sep 19, 1979

MODEL G-61 ULTRASONIC DENTAL UNIT

K791585 · ELC

Dental · 33d

Cleared Aug 22, 1979

MODEL 6500 EXTRACTION IRRIGATION SYS

K791277 · HDQ

Obstetrics & Gynecology · 43d

Cleared Jan 17, 1979

LASER, CO2 SURGICAL

K782054 · HHR

Obstetrics & Gynecology · 41d

Cleared Dec 28, 1978

LASER, PHOTOCOAGULATION

K782065 · HQF

Ophthalmic · 15d

Cleared Sep 14, 1978

AUTO-FIELD II OPHTHALMIC FIELD SCANNER

K781462 · HPT

Ophthalmic · 20d

Cavitron Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Cavitron Corp.

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