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)

FLUORESCENT SUN LAMP FIXTURE

K-Number: K802291 · 1980-10-31

Decision Date1980-10-31
Product CodeHJE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLUORESCENT SUN LAMP FIXTURE is the device name listed in this FDA 510(k) record. The listed applicant is Strato-Ray Co.. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K802291. The device is classified under product code HJE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUORESCENT SUN LAMP FIXTURE?

FLUORESCENT SUN LAMP FIXTURE is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is Strato-Ray Co.. The 510(k) number is K802291.

When did FLUORESCENT SUN LAMP FIXTURE receive FDA 510(k) clearance?

FLUORESCENT SUN LAMP FIXTURE received FDA 510(k) clearance on 1980-10-31, under 510(k) number K802291.

Who is the listed applicant for FLUORESCENT SUN LAMP FIXTURE?

The FDA 510(k) record lists Strato-Ray Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUORESCENT SUN LAMP FIXTURE?

The FDA product code for FLUORESCENT SUN LAMP FIXTURE is HJE.

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.

Other records listing Strato-Ray 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.

Related Devices (Code: HJE)

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.

↑