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FDA 510(k)

ORNITHINE INDOLE MOTILITY

K-Number: K842851 · 1984-08-07

Decision Date1984-08-07
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ORNITHINE INDOLE MOTILITY is the device name listed in this FDA 510(k) record. The listed applicant is Anarobe Systems. It received FDA 510(k) clearance on 1984-08-07 under 510(k) number K842851. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORNITHINE INDOLE MOTILITY?

ORNITHINE INDOLE MOTILITY is a medical device that received FDA 510(k) clearance on 1984-08-07. The listed applicant is Anarobe Systems. The 510(k) number is K842851.

When did ORNITHINE INDOLE MOTILITY receive FDA 510(k) clearance?

ORNITHINE INDOLE MOTILITY received FDA 510(k) clearance on 1984-08-07, under 510(k) number K842851.

Who is the listed applicant for ORNITHINE INDOLE MOTILITY?

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

What is the FDA product code for ORNITHINE INDOLE MOTILITY?

The FDA product code for ORNITHINE INDOLE MOTILITY is JSH.

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 Anarobe Systems 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: JSH)

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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