Blind Controls for Drugs of Abuse Testing

FDA 510(k) K903909 · Rapid Diagnostic Laboratories, Inc.

Substantially Equivalent

510(k) numberK903909

Submission

Device name
Blind Controls for Drugs of Abuse Testing
Applicant
Rapid Diagnostic Laboratories, Inc.
Port Washington, NY, US
Received
August 22, 1990
Decision date
October 26, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DIF – Drug Mixture Control Materials
Device class
Class I (low risk)
Regulation
21 CFR 862.3280
Specialty
Clinical Toxicology

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More from Roche Diagnostics Corp.

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Questions and answers

When was Blind Controls for Drugs of Abuse Testing cleared by the FDA?

Blind Controls for Drugs of Abuse Testing (K903909) received a 510(k) decision of Substantially Equivalent on October 26, 1990, 65 days after the submission was received.

What is the product code of K903909?

The FDA product code is DIF – Drug Mixture Control Materials, a Class I (low risk) device regulated under 21 CFR 862.3280.