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FDA 510(k)

CYSTINE TRYPTIC AGAR W/MALTOSE

K-Number: K844544 · 1985-01-16

Decision Date1985-01-16
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CYSTINE TRYPTIC AGAR W/MALTOSE is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 1985-01-16 under 510(k) number K844544. The device is classified under product code JSF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYSTINE TRYPTIC AGAR W/MALTOSE?

CYSTINE TRYPTIC AGAR W/MALTOSE is a medical device that received FDA 510(k) clearance on 1985-01-16. The listed applicant is bioMerieux, Inc.. The 510(k) number is K844544.

When did CYSTINE TRYPTIC AGAR W/MALTOSE receive FDA 510(k) clearance?

CYSTINE TRYPTIC AGAR W/MALTOSE received FDA 510(k) clearance on 1985-01-16, under 510(k) number K844544.

Who is the listed applicant for CYSTINE TRYPTIC AGAR W/MALTOSE?

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 CYSTINE TRYPTIC AGAR W/MALTOSE?

The FDA product code for CYSTINE TRYPTIC AGAR W/MALTOSE is JSF.

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 bioMerieux, 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.

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Related Devices (Code: JSF)

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

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

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