Medical Device Manufacturer · US , Lake Forest , CA

Sudormed, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1990
6
Total
6
Cleared
0
Denied

Sudormed, Inc. has 6 FDA 510(k) cleared medical devices. Based in Lake Forest, US.

Historical record: 6 cleared submissions from 1990 to 1996. Primary specialty: Toxicology.

Browse the FDA 510(k) cleared devices submitted by Sudormed, Inc. Filter by specialty or product code using the sidebar.

6 devices
1–6 of 6
SUDORMED SWEAT PATCH SPECIMEN CONTAINER FOR COLLECTION OF MARIJUANA IN PERSPIRATION
K936135 · LAT Radioimmunoassay, Cannabinoid(s) · Chemistry
Jun 1996 895d
SUDORMED SWEAT PATCH SPECIMENT CONTAINER (PHENCYCLIDINE)
K936240 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection · Toxicology
Mar 1996 810d
SUDORMED SWEAT PATCH SPECIMEN CONTAINER: COCAINE
K926253 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection · Toxicology
Jul 1995 942d
SUDORMED SWEAT PATCH SPECIMEN CONTAINER FOR COLLECTION OF OPIATES IN PERSPIRATION
K935564 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection · Toxicology
Jul 1995 603d
SUDORMED SWEAT PATCH SPECIMEN CONTAINER FOR COLLECTION OF AMPHETAMINES IN PERSPIRATION
K935588 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection · Toxicology
Jul 1995 604d
SUDORMED SWEAT PATCH SPECIMEN CONTAINER
K902442 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection · Chemistry
Oct 1990 125d
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All6 Toxicology 4 Chemistry 2