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FDA 510(k)

TRYPTIC SOY BROTH

K-Number: K844541 · 1985-01-07

ApplicantbioMerieux, Inc.
Decision Date1985-01-07
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRYPTIC SOY BROTH is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 1985-01-07 under 510(k) number K844541. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRYPTIC SOY BROTH?

TRYPTIC SOY BROTH is a medical device that received FDA 510(k) clearance on 1985-01-07. The listed applicant is bioMerieux, Inc.. The 510(k) number is K844541.

When did TRYPTIC SOY BROTH receive FDA 510(k) clearance?

TRYPTIC SOY BROTH received FDA 510(k) clearance on 1985-01-07, under 510(k) number K844541.

Who is the listed applicant for TRYPTIC SOY BROTH?

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

What is the FDA product code for TRYPTIC SOY BROTH?

The FDA product code for TRYPTIC SOY BROTH is JSG.

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Related Devices (Code: JSG)

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.

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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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