Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BEL O SOL UVA SUNLAMP DEVICE

K-Number: K801149 · 1980-06-30

Decision Date1980-06-30
Product Code
DecisionSubstantially Equivalent

Device Summary

BEL O SOL UVA SUNLAMP DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Hopeful Sunlamp Corp.. It received FDA 510(k) clearance on 1980-06-30 under 510(k) number K801149. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEL O SOL UVA SUNLAMP DEVICE?

BEL O SOL UVA SUNLAMP DEVICE is a medical device that received FDA 510(k) clearance on 1980-06-30. The listed applicant is Hopeful Sunlamp Corp.. The 510(k) number is K801149.

When did BEL O SOL UVA SUNLAMP DEVICE receive FDA 510(k) clearance?

BEL O SOL UVA SUNLAMP DEVICE received FDA 510(k) clearance on 1980-06-30, under 510(k) number K801149.

Who is the listed applicant for BEL O SOL UVA SUNLAMP DEVICE?

The FDA 510(k) record lists Hopeful Sunlamp Corp. 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.

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.

↑