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FDA 510(k)

UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 305

K-Number: K828654 · 1983-01-03

ApplicantDaavlin Co.
Decision Date1983-01-03
Product Code
DecisionSubstantially Equivalent

Device Summary

UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 305 is the device name listed in this FDA 510(k) record. The listed applicant is Daavlin Co.. It received FDA 510(k) clearance on 1983-01-03 under 510(k) number K828654. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 305?

UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 305 is a medical device that received FDA 510(k) clearance on 1983-01-03. The listed applicant is Daavlin Co.. The 510(k) number is K828654.

When did UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 305 receive FDA 510(k) clearance?

UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 305 received FDA 510(k) clearance on 1983-01-03, under 510(k) number K828654.

Who is the listed applicant for UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 305?

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 724K827690SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USE

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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