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)

SUNGLASSES, NON-PRESCRIPTION (ITALO CREMONA)

K-Number: K910126 · 1991-03-14

Decision Date1991-03-14
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUNGLASSES, NON-PRESCRIPTION (ITALO CREMONA) is the device name listed in this FDA 510(k) record. The listed applicant is The Limited Stores, Inc.. It received FDA 510(k) clearance on 1991-03-14 under 510(k) number K910126. 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 SUNGLASSES, NON-PRESCRIPTION (ITALO CREMONA)?

SUNGLASSES, NON-PRESCRIPTION (ITALO CREMONA) is a medical device that received FDA 510(k) clearance on 1991-03-14. The listed applicant is The Limited Stores, Inc.. The 510(k) number is K910126.

When did SUNGLASSES, NON-PRESCRIPTION (ITALO CREMONA) receive FDA 510(k) clearance?

SUNGLASSES, NON-PRESCRIPTION (ITALO CREMONA) received FDA 510(k) clearance on 1991-03-14, under 510(k) number K910126.

Who is the listed applicant for SUNGLASSES, NON-PRESCRIPTION (ITALO CREMONA)?

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

What is the FDA product code for SUNGLASSES, NON-PRESCRIPTION (ITALO CREMONA)?

The FDA product code for SUNGLASSES, NON-PRESCRIPTION (ITALO CREMONA) 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.

Other records listing The Limited Stores, Inc. 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: 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.

↑