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FDA 510(k)

CATION ADJUSTED MUELLER HINTON BROTH

K-Number: K925644 · 1993-01-15

ApplicantPasco Laboratories, Inc.
Decision Date1993-01-15
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CATION ADJUSTED MUELLER HINTON BROTH is the device name listed in this FDA 510(k) record. The listed applicant is Pasco Laboratories, Inc.. It received FDA 510(k) clearance on 1993-01-15 under 510(k) number K925644. 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 CATION ADJUSTED MUELLER HINTON BROTH?

CATION ADJUSTED MUELLER HINTON BROTH is a medical device that received FDA 510(k) clearance on 1993-01-15. The listed applicant is Pasco Laboratories, Inc.. The 510(k) number is K925644.

When did CATION ADJUSTED MUELLER HINTON BROTH receive FDA 510(k) clearance?

CATION ADJUSTED MUELLER HINTON BROTH received FDA 510(k) clearance on 1993-01-15, under 510(k) number K925644.

Who is the listed applicant for CATION ADJUSTED MUELLER HINTON BROTH?

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

What is the FDA product code for CATION ADJUSTED MUELLER HINTON BROTH?

The FDA product code for CATION ADJUSTED MUELLER HINTON BROTH is JWY.

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Other records listing Pasco Laboratories, Inc. as applicant

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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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