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)

SUPERVISOR SUN GOGGLES(TM)

K-Number: K873405 · 1988-01-11

Decision Date1988-01-11
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUPERVISOR SUN GOGGLES(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Eye Communications, Inc.. It received FDA 510(k) clearance on 1988-01-11 under 510(k) number K873405. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERVISOR SUN GOGGLES(TM)?

SUPERVISOR SUN GOGGLES(TM) is a medical device that received FDA 510(k) clearance on 1988-01-11. The listed applicant is Eye Communications, Inc.. The 510(k) number is K873405.

When did SUPERVISOR SUN GOGGLES(TM) receive FDA 510(k) clearance?

SUPERVISOR SUN GOGGLES(TM) received FDA 510(k) clearance on 1988-01-11, under 510(k) number K873405.

Who is the listed applicant for SUPERVISOR SUN GOGGLES(TM)?

The FDA 510(k) record lists Eye Communications, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPERVISOR SUN GOGGLES(TM)?

The FDA product code for SUPERVISOR SUN GOGGLES(TM) is HQY.

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.

Related Devices (Code: HQY)

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.

↑