Medical Device Manufacturer · US , Bethesda , MD

Cryomedical Sciences, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1991

Total

Cleared

Denied

Cryomedical Sciences, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Bethesda, US.

Historical record: 10 cleared submissions from 1991 to 2001.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

Cryomedical Sciences, 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 - Cryomedical Sciences, Inc.

10 devices

1-10 of 10

Cleared Aug 22, 2001

CRYOPLAN SYSTEM

K011073 · GEH

General & Plastic Surgery · 135d

Cleared Sep 08, 1998

ACCUPROBE 800 SERIES MODEL NUMBERS : 810, 820, 830, 840, 850, 860, 870 AND 880

K982055 · GEH

General & Plastic Surgery · 89d

Cleared Jul 17, 1998

CMS BLIZZARD 700 SERIES MODELS 730, 740,750,760,770,780 & 790

K980668 · GEH

General & Plastic Surgery · 147d

Cleared Jul 17, 1998

CMS BLIZZARD 700 SERIES MODELS 710, 711, 712, 720, 721 AND 722

K980670 · GEH

General & Plastic Surgery · 147d

Cleared Nov 21, 1997

ACCUPROBE 450, ACCUPROBE 550/530 AND THE ACCUPROBE 600 SERIES

K973190 · GEI

General & Plastic Surgery · 88d

Cleared Jul 07, 1997

CMS CRYOLITE

K970995 · GEH

General & Plastic Surgery · 110d

Cleared Mar 20, 1997

CMS ACCUPROBE 610, 620, 630, 640, 650, 660, 670, 680

K964336 · GEH

General & Plastic Surgery · 140d

Cleared Dec 04, 1995

CMS ACCUPROBE 550/530

K953637 · GEH

General & Plastic Surgery · 124d

Cleared Oct 24, 1995

CMS URETHRAL WARMER

K952895 · GEH

General & Plastic Surgery · 123d

Cleared Apr 08, 1991

CMS ONCOPROBE (TM)

K904421 · GEH

General & Plastic Surgery · 193d

Cryomedical Sciences, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Cryomedical Sciences, Inc.

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