Cher Mel Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cher Mel Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Cher Mel Corp. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1984 to 1986. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cher Mel Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cher Mel Corp.
7 devices
Cleared
Oct 31, 1986
DISPOSABLE INTRAVENOUS HYPERALIMENTATION BAGS
General Hospital
80d
Cleared
Aug 23, 1985
CHERMEL SCALP VEIN SET
General Hospital
130d
Cleared
Jun 06, 1985
LITTMAN TYPE SH-6010, NURSE TYPE
Cardiovascular
367d
Cleared
Jun 06, 1985
SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH
Cardiovascular
286d
Cleared
Aug 02, 1984
CHERMEL BONE GOUGES
General & Plastic Surgery
14d
Cleared
Aug 02, 1984
CHERMEL OSTEOTOMES
General & Plastic Surgery
14d
Cleared
Aug 02, 1984
CHERMEL BONE CHISELS
General & Plastic Surgery
14d