Cryomedical Sciences, Inc. is one of 9755 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cryomedical Sciences, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ACCUPROBE 800 SERIES MODEL NUMBERS : 810, 820, 830, 840, 850, 860, 870 AND 880, CMS BLIZZARD 700 SERIES MODELS 730, 740,750,760,770,780 & 790, CMS BLIZZARD 700 SERIES MODELS 710, 711, 712, 720, 721 AND 722
10
Total
10
Cleared
0
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.
FDA 510(k) Regulatory Record - Cryomedical Sciences, Inc.
10 devices
Cleared
Aug 22, 2001
CRYOPLAN SYSTEM
General & Plastic Surgery
135d
Cleared
Sep 08, 1998
ACCUPROBE 800 SERIES MODEL NUMBERS : 810, 820, 830, 840, 850, 860, 870 AND 880
General & Plastic Surgery
89d
Cleared
Jul 17, 1998
CMS BLIZZARD 700 SERIES MODELS 730, 740,750,760,770,780 & 790
General & Plastic Surgery
147d
Cleared
Jul 17, 1998
CMS BLIZZARD 700 SERIES MODELS 710, 711, 712, 720, 721 AND 722
General & Plastic Surgery
147d
Cleared
Nov 21, 1997
ACCUPROBE 450, ACCUPROBE 550/530 AND THE ACCUPROBE 600 SERIES
General & Plastic Surgery
88d
Cleared
Jul 07, 1997
CMS CRYOLITE
General & Plastic Surgery
110d
Cleared
Mar 20, 1997
CMS ACCUPROBE 610, 620, 630, 640, 650, 660, 670, 680
General & Plastic Surgery
140d
Cleared
Dec 04, 1995
CMS ACCUPROBE 550/530
General & Plastic Surgery
124d
Cleared
Oct 24, 1995
CMS URETHRAL WARMER
General & Plastic Surgery
123d
Cleared
Apr 08, 1991
CMS ONCOPROBE (TM)
General & Plastic Surgery
193d