Pasco Mic and Mic/Id Panels

FDA 510(k) K973695 · Pasco Laboratories, Inc.

Substantially Equivalent

510(k) numberK973695

Submission

Device name
Pasco Mic and Mic/Id Panels
Applicant
Pasco Laboratories, Inc.
Wheat Ridge, CO, US
Received
September 26, 1997
Decision date
November 5, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JWY – Manual Antimicrobial Susceptibility Test Systems
Device class
Class II (moderate risk)
Regulation
21 CFR 866.1640
Specialty
Microbiology

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More from Biomérieux

510(k)DeviceDecision
K042331Pasco Mic and Mic/Id PanelsJWY · Traditional 10/07/2004SE
K041776Pasco Mic and Mic/Id PanelsJWY · Traditional 08/03/2004SE
K041214Pasco Mic and Mic/Id PanelsJWY · Traditional 06/07/2004SE
K033119Pasco Mic and Mic/Id PanelsJWY · Traditional 11/18/2003SE
K031727Pasco Mic and Mic/Id Panels, GemifloxacinJWY · Traditional 07/30/2003SE
K031205Pasco Mic and Mic/Id PanelsJWY · Traditional 06/13/2003SE
K031103Pasco Mic and Mic/Id Panels (Ertapenem)JWY · Traditional 06/12/2003SE
K030933Pasco Mic and Mic/Id PanelsJWY · Traditional 05/01/2003SE
K030620Pasco Mic and Mic/Id PanelsLTT · Traditional 04/14/2003SE
K020331Pasco Mic and Mic/Id PanelsJWY · Traditional 03/20/2002SE

Questions and answers

When was Pasco Mic and Mic/Id Panels cleared by the FDA?

Pasco Mic and Mic/Id Panels (K973695) received a 510(k) decision of Substantially Equivalent on November 5, 1997, 40 days after the submission was received.

What is the product code of K973695?

The FDA product code is JWY – Manual Antimicrobial Susceptibility Test Systems, a Class II (moderate risk) device regulated under 21 CFR 866.1640.