Extracorporeal Medical Specialities, Inc. - FDA 510(k) Cleared Devices
69
Total
69
Cleared
0
Denied
Extracorporeal Medical Specialities, Inc. has 69 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.
Historical record: 69 cleared submissions from 1976 to 1984.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Extracorporeal Medical Specialities, Inc.
69 devices
Cleared
Nov 29, 1984
EXTRACORPOREAL MAXIMA HOLLOW FIBER OXYGENATOR
Cardiovascular
51d
Cleared
May 30, 1984
HANCOCK PERICARDIAL PATCH
Cardiovascular
132d
Cleared
May 30, 1984
HEMOPERFUSION SYSTEM TP-400
Gastroenterology & Urology
119d
Cleared
Feb 04, 1984
EXP* 500 PARALLEL PLATE DIALYZER
Gastroenterology & Urology
26d
Cleared
Feb 04, 1984
EXP* 700 PARALLEL PLATE DIALYZER
Gastroenterology & Urology
22d
Cleared
Jan 03, 1984
THERAPEUTIC EXCHANGE SYSTEM
Gastroenterology & Urology
245d
Cleared
Jan 03, 1984
ULTRAFILTRATION CONTROLLER
Gastroenterology & Urology
155d
Cleared
Dec 27, 1983
INTERSEPT 40 MICRON FILTER W/TUBING
Cardiovascular
81d
Cleared
Dec 27, 1983
INTERSEPT 40 MICRON FILTER
Cardiovascular
81d
Cleared
Oct 14, 1983
THERAPEUTIC EXCHANGE BLOOD TUBING-TP-101
Gastroenterology & Urology
164d
Cleared
Sep 29, 1983
SINGLE PATIENT SYS. II MODEL DM-450
Gastroenterology & Urology
94d
Cleared
Aug 31, 1983
HANCOCK PERICARDIAL PATCH
Cardiovascular
166d
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