Multistat III X-Hbdh Test

FDA 510(k) K771474 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK771474

Submission

Device name
Multistat III X-Hbdh Test
Applicant
Instrumentation Laboratory CO
Mchenry, IL, US
Received
August 4, 1977
Decision date
September 13, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JMK – Acid, Alpha-Ketobutyric And Nadh (U.V.), Hydroxybutyric Dehydrogenase
Device class
Class I (low risk)
Regulation
21 CFR 862.1380
Specialty
Clinical Chemistry

Other 510(k)s with product code JMK

510(k)DeviceApplicantDecision
K983860MTM Bioscanner K Test Strips, Cat # BSA610JMK · Traditional Polymer Technology Systems, Inc.12/27/1999SE
K981865MTM Bioscanner K Test StripsJMK · Traditional Polymer Technology Systems, Inc.02/26/1999SE
K953452Ketorex C SanwaJMK · Traditional Ihara Medics U.S., Inc.05/02/1996SE
K941427Serum @-Hydroxybutyrate Dehydrogenase (HBDH)JMK · Traditional Teco Diagnostics03/13/1995SE
K862319HBDH (Optimized) ReagentJMK · Traditional Sigma Chemical Co.07/07/1986SE
K843774Raichem X-Hbdh ReagentJMK · Traditional Reagents Applications, Inc.10/31/1984SE
K822739AhbdJMK · Traditional Gilford Diagnostics10/18/1982SE
K821877Ultrazyme Plus HBDJMK · Traditional Harleco Diagnostics07/14/1982SE
K781720HBDH Enzyme Kinetic Reagent SetJMK · Traditional Medical Analysis Systems, Inc.11/03/1978SE
K780104Ultrazyme Plus HBDJMK · Traditional Harleco02/13/1978SE

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Questions and answers

When was Multistat III X-Hbdh Test cleared by the FDA?

Multistat III X-Hbdh Test (K771474) received a 510(k) decision of Substantially Equivalent on September 13, 1977, 40 days after the submission was received.

What is the product code of K771474?

The FDA product code is JMK – Acid, Alpha-Ketobutyric And Nadh (U.V.), Hydroxybutyric Dehydrogenase, a Class I (low risk) device regulated under 21 CFR 862.1380.