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FDA 510(k)

SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USE

K-Number: K827690 · 1982-10-05

ApplicantDaavlin Co.
Decision Date1982-10-05
Product Code
DecisionSubstantially Equivalent

Device Summary

SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USE is the device name listed in this FDA 510(k) record. The listed applicant is Daavlin Co.. It received FDA 510(k) clearance on 1982-10-05 under 510(k) number K827690. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USE?

SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USE is a medical device that received FDA 510(k) clearance on 1982-10-05. The listed applicant is Daavlin Co.. The 510(k) number is K827690.

When did SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USE receive FDA 510(k) clearance?

SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USE received FDA 510(k) clearance on 1982-10-05, under 510(k) number K827690.

Who is the listed applicant for SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USE?

The FDA 510(k) record lists Daavlin Co. 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 Daavlin Co. 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.

K0636213 SERIES PHOTOTHERAPY CABINETK930856PSORALITEK854498SPECTRA 724K828654UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 305

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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