Visualine II Cannabinoids (THC)

FDA 510(k) K950445 · Sun Biomedical Laboratories, Inc.

Substantially Equivalent

510(k) numberK950445

Submission

Device name
Visualine II Cannabinoids (THC)
Applicant
Sun Biomedical Laboratories, Inc.
Cherry Hill, NJ, US
Received
January 27, 1995
Decision date
May 2, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LDJ – Enzyme Immunoassay, Cannabinoids
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3870
Specialty
Clinical Toxicology

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Questions and answers

When was Visualine II Cannabinoids (THC) cleared by the FDA?

Visualine II Cannabinoids (THC) (K950445) received a 510(k) decision of Substantially Equivalent on May 2, 1995, 95 days after the submission was received.

What is the product code of K950445?

The FDA product code is LDJ – Enzyme Immunoassay, Cannabinoids, a Class II (moderate risk) device regulated under 21 CFR 862.3870.