Medical Device Manufacturer · US , Walker , MI

Frigitronics of Connecticut, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1976

Total

Cleared

Denied

Frigitronics of Connecticut, Inc. has 9 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 9 cleared submissions from 1976 to 1989. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Frigitronics of Connecticut, Inc. Filter by specialty or product code using the sidebar.

Frigitronics of Connecticut, Inc. 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 - Frigitronics of Connecticut, Inc.

9 devices

1-9 of 9

Cleared Jun 15, 1989

MIC-100 WITH CRYOPROBES

K891282 · GEH

General & Plastic Surgery · 98d

Cleared Jul 27, 1987

FRIGITRONICS ACC-1000 CAPSULE CUTTER

K872362 · HQC

Ophthalmic · 39d

Cleared Oct 04, 1985

KEATES IRRIGATION/ASPIRATION/VITREOUS CUTTER 5000

General & Plastic Surgery · 145d

Cleared Apr 23, 1984

CRYO SURG 5900

K840536 · GEH

General & Plastic Surgery · 75d

Cleared Mar 30, 1984

KEATES IRRIGATION/ASPIRATION/VITREOUS

K834437 · HQE

Ophthalmic · 102d

Cleared Oct 06, 1982

KEATES I/A SYSTEM FRIGITRONICS 4000

K822599 · HKP

Ophthalmic · 40d

Cleared Jun 16, 1981

CCS100 CRYOSURGICAL SYSTEM

K811390 · GEH

General & Plastic Surgery · 29d

Cleared Nov 03, 1976

CS-76 AND/OR CRYOCARE I

K760742 · GEH

General & Plastic Surgery · 34d

Frigitronics of Connecticut, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Frigitronics of Connecticut, Inc.

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