Liquid TDM Controls

FDA 510(k) K871788 · Biological Industries

Substantially Equivalent

510(k) numberK871788

Submission

Device name
Liquid TDM Controls
Applicant
Biological Industries
25115, IL
Received
May 6, 1987
Decision date
June 17, 1987
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 Liquid TDM Controls cleared by the FDA?

Liquid TDM Controls (K871788) received a 510(k) decision of Substantially Equivalent on June 17, 1987, 42 days after the submission was received.

What is the product code of K871788?

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