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FDA 510(k)

ADDVANTAGE:TVC MARCON

K-Number: K880284 · 1988-02-26

Decision Date1988-02-26
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ADDVANTAGE:TVC MARCON is the device name listed in this FDA 510(k) record. The listed applicant is Richards Medical Co., Inc.. It received FDA 510(k) clearance on 1988-02-26 under 510(k) number K880284. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADDVANTAGE:TVC MARCON?

ADDVANTAGE:TVC MARCON is a medical device that received FDA 510(k) clearance on 1988-02-26. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K880284.

When did ADDVANTAGE:TVC MARCON receive FDA 510(k) clearance?

ADDVANTAGE:TVC MARCON received FDA 510(k) clearance on 1988-02-26, under 510(k) number K880284.

Who is the listed applicant for ADDVANTAGE:TVC MARCON?

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

What is the FDA product code for ADDVANTAGE:TVC MARCON?

The FDA product code for ADDVANTAGE:TVC MARCON is ESD.

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 Richards Medical Co., 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.

View all 71 devices →

Related Devices (Code: ESD)

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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