FDA 510(k)

DERMALIGHT BLUE-POINT

K-Number: K828674 · 1983-01-17

Decision Date1983-01-17

Product Code

DecisionSubstantially Equivalent

Device Summary

DERMALIGHT BLUE-POINT is the device name listed in this FDA 510(k) record. The listed applicant is Dr. K. Honle GmbH. It received FDA 510(k) clearance on 1983-01-17 under 510(k) number K828674. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMALIGHT BLUE-POINT?

DERMALIGHT BLUE-POINT is a medical device that received FDA 510(k) clearance on 1983-01-17. The listed applicant is Dr. K. Honle GmbH. The 510(k) number is K828674.

When did DERMALIGHT BLUE-POINT receive FDA 510(k) clearance?

DERMALIGHT BLUE-POINT received FDA 510(k) clearance on 1983-01-17, under 510(k) number K828674.

Who is the listed applicant for DERMALIGHT BLUE-POINT?

The FDA 510(k) record lists Dr. K. Honle GmbH 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 Dr. K. Honle GmbH as applicant

K828676DERMALIGHT SPOT K828675DERMALIGHT UVASTAR 400

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.