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FDA 510(k)

SOLARIUM COMBINATION

K-Number: K812663 · 1981-10-29

ApplicantTech-Pro, Inc.
Decision Date1981-10-29
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SOLARIUM COMBINATION is the device name listed in this FDA 510(k) record. The listed applicant is Tech-Pro, Inc.. It received FDA 510(k) clearance on 1981-10-29 under 510(k) number K812663. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLARIUM COMBINATION?

SOLARIUM COMBINATION is a medical device that received FDA 510(k) clearance on 1981-10-29. The listed applicant is Tech-Pro, Inc.. The 510(k) number is K812663.

When did SOLARIUM COMBINATION receive FDA 510(k) clearance?

SOLARIUM COMBINATION received FDA 510(k) clearance on 1981-10-29, under 510(k) number K812663.

Who is the listed applicant for SOLARIUM COMBINATION?

The FDA 510(k) record lists Tech-Pro, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOLARIUM COMBINATION?

The FDA product code for SOLARIUM COMBINATION is FTC.

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Related Devices (Code: FTC)

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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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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