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FDA 510(k)

FOX FASTIDIOUS TEST PANELS

K-Number: K953422 · 1995-10-07

Decision Date1995-10-07
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

FOX FASTIDIOUS TEST PANELS is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Media Systems, Inc.. It received FDA 510(k) clearance on 1995-10-07 under 510(k) number K953422. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOX FASTIDIOUS TEST PANELS?

FOX FASTIDIOUS TEST PANELS is a medical device that received FDA 510(k) clearance on 1995-10-07. The listed applicant is Micro-Media Systems, Inc.. The 510(k) number is K953422.

When did FOX FASTIDIOUS TEST PANELS receive FDA 510(k) clearance?

FOX FASTIDIOUS TEST PANELS received FDA 510(k) clearance on 1995-10-07, under 510(k) number K953422.

Who is the listed applicant for FOX FASTIDIOUS TEST PANELS?

The FDA 510(k) record lists Micro-Media Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FOX FASTIDIOUS TEST PANELS?

The FDA product code for FOX FASTIDIOUS TEST PANELS is JWY.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Micro-Media Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 7 devices →

Related Devices (Code: JWY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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