ANNE MARIE PERRIS SUNGLASSES AND FRAMES
K-Number: K851698 · 1985-07-31
Advertisement
Device Summary
Frequently Asked Questions
What is the ANNE MARIE PERRIS SUNGLASSES AND FRAMES?
ANNE MARIE PERRIS SUNGLASSES AND FRAMES is a medical device that received FDA 510(k) clearance on 1985-07-31. The listed applicant is Perlinea Co.. The 510(k) number is K851698.
When did ANNE MARIE PERRIS SUNGLASSES AND FRAMES receive FDA 510(k) clearance?
ANNE MARIE PERRIS SUNGLASSES AND FRAMES received FDA 510(k) clearance on 1985-07-31, under 510(k) number K851698.
Who is the listed applicant for ANNE MARIE PERRIS SUNGLASSES AND FRAMES?
The FDA 510(k) record lists Perlinea Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANNE MARIE PERRIS SUNGLASSES AND FRAMES?
The FDA product code for ANNE MARIE PERRIS SUNGLASSES AND FRAMES 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