Pyrilinks Assay Kit

FDA 510(k) K952506 · Metra Biosystems, Inc.

Substantially Equivalent

510(k) numberK952506

Submission

Device name
Pyrilinks Assay Kit
Applicant
Metra Biosystems, Inc.
Laurel, MD, US
Received
May 31, 1995
Decision date
November 3, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JMM – Column Chromatography & Color Development, Hydroxyproline
Device class
Class I (low risk)
Regulation
21 CFR 862.1400
Specialty
Clinical Chemistry

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K992997Osteomark NTX PocJMM · Traditional Metrika, Inc.11/09/1999SE
K990843Serum Crosslaps One Step ElisaJMM · Traditional Osteometer Biotech A/S07/09/1999SE
K983457Osteomark NTX Serum EiaJMM · Traditional Ostex Intl., Inc.02/02/1999SE
K983674Vitros Immunodiagnostic Products: NTX Calibrators, NTX Reagent Pack, NTX ControlsJMM · Traditional Ortho-Clinical Diagnostics, Inc.01/29/1999SE
K972788Crosslaps ElisaJMM · Traditional Devices and Diagnostics Consulting Group12/22/1998SE
K981364Pyrilinks-D Assay KitJMM · Traditional Metra Biosystems, Inc.08/13/1998SE
K980833Immulite Pyrilinks-D Model Numbers LKPD1, LKPD5JMM · Traditional Diagnostic Products Corp.05/01/1998SE
K980518OsteomarkJMM · Traditional Ostex Intl., Inc.03/06/1998SE

More from Ostex Intl., Inc.

510(k)DeviceDecision
K981364Pyrilinks-D Assay KitJMM · Traditional 08/13/1998SE
K981373Alkphase-B Assay KitCIN · Traditional 05/27/1998SE
K974260Pyrilinks-D Assay KitJMM · Traditional 01/26/1998SE
K952320Pyrilinks-D Assay KitJMM · Traditional 12/29/1995SE
K952026Pyrilinks Polyclonal Assay KitJMM · Traditional 11/03/1995SE
K952768Alkphase-B Assay KitCIN · Traditional 08/24/1995SE

Questions and answers

When was Pyrilinks Assay Kit cleared by the FDA?

Pyrilinks Assay Kit (K952506) received a 510(k) decision of Substantially Equivalent on November 3, 1995, 156 days after the submission was received.

What is the product code of K952506?

The FDA product code is JMM – Column Chromatography & Color Development, Hydroxyproline, a Class I (low risk) device regulated under 21 CFR 862.1400.