SINCLAIR NON-PRESCRIPTION SUNGLASSES
K-Number: K954393 · 1995-10-25
Advertisement
Device Summary
Frequently Asked Questions
What is the SINCLAIR NON-PRESCRIPTION SUNGLASSES?
SINCLAIR NON-PRESCRIPTION SUNGLASSES is a medical device that received FDA 510(k) clearance on 1995-10-25. The listed applicant is Sinclair Corp.. The 510(k) number is K954393.
When did SINCLAIR NON-PRESCRIPTION SUNGLASSES receive FDA 510(k) clearance?
SINCLAIR NON-PRESCRIPTION SUNGLASSES received FDA 510(k) clearance on 1995-10-25, under 510(k) number K954393.
Who is the listed applicant for SINCLAIR NON-PRESCRIPTION SUNGLASSES?
The FDA 510(k) record lists Sinclair Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SINCLAIR NON-PRESCRIPTION SUNGLASSES?
The FDA product code for SINCLAIR NON-PRESCRIPTION SUNGLASSES 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.
Advertisement