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FDA 510(k)

TANARAMA

K-Number: K812603 · 1981-11-20

ApplicantMarketing Consultants of America
Decision Date1981-11-20
Product CodeGGG
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TANARAMA is the device name listed in this FDA 510(k) record. The listed applicant is Marketing Consultants of America. It received FDA 510(k) clearance on 1981-11-20 under 510(k) number K812603. The device is classified under product code GGG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TANARAMA?

TANARAMA is a medical device that received FDA 510(k) clearance on 1981-11-20. The listed applicant is Marketing Consultants of America. The 510(k) number is K812603.

When did TANARAMA receive FDA 510(k) clearance?

TANARAMA received FDA 510(k) clearance on 1981-11-20, under 510(k) number K812603.

Who is the listed applicant for TANARAMA?

The FDA 510(k) record lists Marketing Consultants of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TANARAMA?

The FDA product code for TANARAMA is GGG.

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Other records listing Marketing Consultants of America 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.

K812543TANARAMA

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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