Polamedco, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Polamedco, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Polamedco, Inc. has 20 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 20 cleared submissions from 1978 to 1999.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Polamedco, Inc.
20 devices
Cleared
Oct 27, 1999
CRICOTHYROTOMY TUBE
Anesthesiology
426d
Cleared
Dec 22, 1995
SURELOC CIRCUIT CONNECTOR
Anesthesiology
94d
Cleared
Nov 29, 1995
INTROSCOPE
Anesthesiology
107d
Cleared
May 17, 1995
AIRGUIDE STYLETTE
Anesthesiology
91d
Cleared
Feb 13, 1995
GASTRIC, CATHETER, IRRIGATION & ASPIRATION
Gastroenterology & Urology
567d
Cleared
Feb 10, 1995
FLEXTITIP STYLETTE
Anesthesiology
10d
Cleared
Mar 18, 1992
POLAMEDCO TRACHEAL AND NASOTRACHEAL TUBES
Anesthesiology
21d
Cleared
Apr 19, 1990
POLAMEDCO NASOPAHARYNGEAL AIRWAY
Anesthesiology
79d
Cleared
Apr 16, 1990
CUFFED LINDER NASOTRACHEAL AIRWAY
Anesthesiology
76d
Cleared
Sep 12, 1989
VISOSHIELD(TM), SURGICAL EYE PROTECTOR
General Hospital
55d
Cleared
May 31, 1988
LINDER NASOTRACHEAL AIRWAY
Anesthesiology
53d
Cleared
Oct 04, 1984
LINDER NASOPHARYNGEAL AIRWAY
Anesthesiology
28d