STC Diagnostics Auto-Lyte Benzodiazepines Eia

FDA 510(k) K934869 · Solarcare Technologies Corp,Inc.

Substantially Equivalent

510(k) numberK934869

Submission

Device name
STC Diagnostics Auto-Lyte Benzodiazepines Eia
Applicant
Solarcare Technologies Corp,Inc.
Bethlehem, PA, US
Received
October 12, 1993
Decision date
November 22, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JXM – Enzyme Immunoassay, Benzodiazepine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3170
Specialty
Clinical Toxicology

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More from Healgen Scientific,, LLC

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K954326STC Diagnostics Auto-Lyte Urinary Hemoglobin AssayJIT · Traditional 07/23/1996SE
K954156STC Diagnostics Auto-Lyte Urinary Leukocyte Esterase AssayKQO · Traditional 07/22/1996SE
K955905STC Diagnostics Auto-Lyte Urinary Protein AssayCEK · Traditional 05/30/1996SE
K954158STC Diagnostics Auto-Lyte PH AssayKQO · Traditional 04/30/1996SE
K940048STC Diagnostics PCP Micro-Plate Eia ModificationDLJ · Traditional 03/19/1996SE
K954073STC Diagnostics LSD Micro-Plate EiaDLB · Traditional 11/29/1995SE
K954266STC Diagnostics Auto-Lyte Creatinine AssayCGX · Traditional 10/13/1995SE
K935573Amphetamines Micro-Plate EiaDKZ · Traditional 07/14/1995SE
K935565Opiates Micro-Plate AssayDJG · Traditional 07/14/1995SE
K950308STC Diagnostics Auto-Lyte(R) Methaqualone EiaJXS · Traditional 04/14/1995SE

Questions and answers

When was STC Diagnostics Auto-Lyte Benzodiazepines Eia cleared by the FDA?

STC Diagnostics Auto-Lyte Benzodiazepines Eia (K934869) received a 510(k) decision of Substantially Equivalent on November 22, 1993, 41 days after the submission was received.

What is the product code of K934869?

The FDA product code is JXM – Enzyme Immunoassay, Benzodiazepine, a Class II (moderate risk) device regulated under 21 CFR 862.3170.