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FDA 510(k)

SOLARIUM, MODEL 6040A

K-Number: K800366 · 1980-06-17

ApplicantBlendette Intl. , Ltd.
Decision Date1980-06-17
Product Code
DecisionSubstantially Equivalent

Device Summary

SOLARIUM, MODEL 6040A is the device name listed in this FDA 510(k) record. The listed applicant is Blendette Intl. , Ltd.. It received FDA 510(k) clearance on 1980-06-17 under 510(k) number K800366. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLARIUM, MODEL 6040A?

SOLARIUM, MODEL 6040A is a medical device that received FDA 510(k) clearance on 1980-06-17. The listed applicant is Blendette Intl. , Ltd.. The 510(k) number is K800366.

When did SOLARIUM, MODEL 6040A receive FDA 510(k) clearance?

SOLARIUM, MODEL 6040A received FDA 510(k) clearance on 1980-06-17, under 510(k) number K800366.

Who is the listed applicant for SOLARIUM, MODEL 6040A?

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

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.

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Other records listing Blendette Intl. , 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.

K801181VAP 2001

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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