STC DIAGNOSTICS AUTO-LYTE AMPHETAMINES EIA— 510(k) K930690

Name: FDA 510(k) clearance K930690
Creator: U.S. Food and Drug Administration
Published: 1993-04-16

Substantially Equivalent

Solarcare Technologies Corp,Inc.

FDA 510(k) clearance K930690 for STC DIAGNOSTICS AUTO-LYTE AMPHETAMINES EIA, Substantially Equivalent on 1993-04-16. Applicant: Solarcare Technologies Corp,Inc.. Device class: 2.

Clearance details

Applicant: Solarcare Technologies Corp,Inc.
Product code: Code DKZ
Device class: Class 2
Regulation: 21 CFR 862.3100
Advisory panel: Clinical Toxicology
Date received: 1993-02-10
Decision date: 1993-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethlehem, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DKZ

view all

K240670 — DRI Ecstasy Plus Assay2024-10-30
K233019 — AllTest Multi-Drug Rapid Test Cup +3 more2023-12-13
K231137 — Xenta Drug Screen Cup, Xenta Drug Screen Dipcard2023-05-19
K200363 — Quidel Triage® TOX Drug Screen, 946002020-03-11
K191099 — Atlas Multi-Drugs Screening Test Cup, Atlas Multi-Drugs Screening Test Panel2019-10-03

More clearances from Solarcare Technologies Corp,Inc.

view all

K954326 — STC DIAGNOSTICS AUTO-LYTE URINARY HEMOGLOBIN ASSAY1996-07-23
K954156 — STC DIAGNOSTICS AUTO-LYTE URINARY LEUKOCYTE ESTERASE ASSAY1996-07-22
K955905 — STC DIAGNOSTICS AUTO-LYTE URINARY PROTEIN ASSAY1996-05-30
K954158 — STC DIAGNOSTICS AUTO-LYTE PH ASSAY1996-04-30
K940048 — STC DIAGNOSTICS PCP MICRO-PLATE EIA MODIFICATION1996-03-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.