Vancomycin Flex Reagent Cartridge

FDA 510(k) K963267 · Dade Intl., Inc.

Substantially Equivalent

510(k) numberK963267

Submission

Device name
Vancomycin Flex Reagent Cartridge
Applicant
Dade Intl., Inc.
Newark, DE, US
Received
August 20, 1996
Decision date
September 13, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LEH – Radioimmunoassay, Vancomycin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3950
Specialty
Clinical Toxicology

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K032811Cedia Vancomycin AssayLEH · Traditional Microgenics Corp.11/24/2003SE

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Questions and answers

When was Vancomycin Flex Reagent Cartridge cleared by the FDA?

Vancomycin Flex Reagent Cartridge (K963267) received a 510(k) decision of Substantially Equivalent on September 13, 1996, 24 days after the submission was received.

What is the product code of K963267?

The FDA product code is LEH – Radioimmunoassay, Vancomycin, a Class II (moderate risk) device regulated under 21 CFR 862.3950.