Arbrook Mfg. Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arbrook Mfg. Corp. General Hospital ✕
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