Solarcare, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Solarcare, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Solarcare, Inc. has 6 FDA 510(k) cleared medical devices. Based in Bethlehem, US.
Historical record: 6 cleared submissions from 1993 to 1995. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Solarcare, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Solarcare, Inc.
6 devices
Cleared
Jul 14, 1995
STC COCAINE METABOLITE EIA
Toxicology
647d
Cleared
Feb 08, 1995
STC DIAGNOSTIC AUTO-LYTE PROPOXYPHENE EIA
Toxicology
154d
Cleared
Oct 27, 1994
SOLARCARE TOTAL PROTEIN MICRO-PLATE ASSAY
Chemistry
213d
Cleared
May 24, 1994
SOLARCARE ALANINE AMINOTRANSFERASE MICRO-PLATE ASSAY
Chemistry
57d
Cleared
Dec 07, 1993
STC DIAGNOSTICS AUTO-LYTE BARBITURATES EIA
Toxicology
89d
Cleared
Oct 29, 1993
HISTOFREEZER
General & Plastic Surgery
113d