Tomarc (M) Sdn Bhd is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Tomarc (M) Sdn Bhd - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Tomarc (M) Sdn Bhd has 5 FDA 510(k) cleared medical devices. Based in Kuala Lumpar, MY.
Historical record: 5 cleared submissions from 1989 to 1993. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tomarc (M) Sdn Bhd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tomarc (M) Sdn Bhd
5 devices
Cleared
Oct 25, 1993
POWDER-FREE LATEX PATIENT EXAMINATION GLOVES
General Hospital
206d
Cleared
Jul 23, 1993
STERILE HYPOALLERGENIC POWDER-FREE LATEX SURG. GLV
General Hospital
368d
Cleared
Jan 17, 1990
STERILE LATEX SURGICAL GLOVE
General Hospital
272d
Cleared
May 12, 1989
LATEX DECONTAMINATION/PROCEDURE GLOVES (NON-STER)
General Hospital
105d
Cleared
Apr 26, 1989
GLOVES, PATIENT EXAMINATION
Microbiology
93d