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FDA 510(k)

CAMPYLOCACTER SUPPLEMENT

K-Number: K843653 · 1984-10-23

Decision Date1984-10-23
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CAMPYLOCACTER SUPPLEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Institute Virion , Ltd.. It received FDA 510(k) clearance on 1984-10-23 under 510(k) number K843653. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMPYLOCACTER SUPPLEMENT?

CAMPYLOCACTER SUPPLEMENT is a medical device that received FDA 510(k) clearance on 1984-10-23. The listed applicant is Institute Virion , Ltd.. The 510(k) number is K843653.

When did CAMPYLOCACTER SUPPLEMENT receive FDA 510(k) clearance?

CAMPYLOCACTER SUPPLEMENT received FDA 510(k) clearance on 1984-10-23, under 510(k) number K843653.

Who is the listed applicant for CAMPYLOCACTER SUPPLEMENT?

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

What is the FDA product code for CAMPYLOCACTER SUPPLEMENT?

The FDA product code for CAMPYLOCACTER SUPPLEMENT is JSJ.

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 Institute Virion , Ltd. 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 16 devices →

Related Devices (Code: JSJ)

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

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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