Arbrook Mfg. Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arbrook Mfg. Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Arbrook Mfg. Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1976 to 1979. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Arbrook Mfg. Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arbrook Mfg. Corp.
5 devices
Cleared
Oct 26, 1979
DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL
General Hospital
21d
Cleared
Nov 03, 1978
LATEX, IN-HOUSE COMPOUNDED
General Hospital
1d
Cleared
Aug 31, 1978
GLOVES, PROCEDURE
General Hospital
37d
Cleared
Feb 25, 1977
GLOVES, SURGEONS,MICRO-TOUCH POWDERFREE
General Hospital
45d
Cleared
Aug 23, 1976
THERMOMETER, SURVALENT-ELECTRONIC
General Hospital
13d