Cranberry (M) Sdn. Bhd. is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Cranberry (M) Sdn. Bhd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cranberry (M) Sdn. Bhd. has 4 FDA 510(k) cleared medical devices. Based in Ipoh Perak, MY.
Historical record: 4 cleared submissions from 1989 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Cranberry (M) Sdn. Bhd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cranberry (M) Sdn. Bhd.
4 devices
Cleared
Mar 29, 1999
CRANBERRY POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING...
General Hospital
137d
Cleared
Feb 19, 1999
NITRILE POWDER FREE EXAMINATION GLOVES
General Hospital
149d
Cleared
Jun 21, 1994
POWDER FREE LATEX EXAMINATION GLOVES
General Hospital
190d
Cleared
Apr 18, 1989
PATIENT EXAMINATION GLOVE
General Hospital
50d