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FDA 510(k)

MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE

K-Number: K896566 · 1990-02-09

ApplicantMedical Specialties, Inc.
Decision Date1990-02-09
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Specialties, Inc.. It received FDA 510(k) clearance on 1990-02-09 under 510(k) number K896566. 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 MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE?

MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE is a medical device that received FDA 510(k) clearance on 1990-02-09. The listed applicant is Medical Specialties, Inc.. The 510(k) number is K896566.

When did MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE receive FDA 510(k) clearance?

MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE received FDA 510(k) clearance on 1990-02-09, under 510(k) number K896566.

Who is the listed applicant for MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE?

The FDA 510(k) record lists Medical Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE?

The FDA product code for MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE is JWY.

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Other records listing Medical Specialties, 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.

K946201STAND, INFUSIONK931947CHECKPOINTK926095REFRACTROL-SPK924926MSI-HCTK883851MSI-CAL 8K883703MSI-CAL 7

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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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