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FDA 510(k)

MRVP BROTH

K-Number: K880116 · 1988-03-31

ApplicantHardy Media
Decision Date1988-03-31
Product CodeJSE
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MRVP BROTH is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Media. It received FDA 510(k) clearance on 1988-03-31 under 510(k) number K880116. The device is classified under product code JSE. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MRVP BROTH?

MRVP BROTH is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Hardy Media. The 510(k) number is K880116.

When did MRVP BROTH receive FDA 510(k) clearance?

MRVP BROTH received FDA 510(k) clearance on 1988-03-31, under 510(k) number K880116.

Who is the listed applicant for MRVP BROTH?

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

What is the FDA product code for MRVP BROTH?

The FDA product code for MRVP BROTH is JSE.

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 Hardy Media 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: JSE)

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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