MODEL F 1 FLIP-UP SUNGLASSES W/POLORIZED LENS
K-Number: K900526 · 1990-05-03
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Device Summary
Frequently Asked Questions
What is the MODEL F 1 FLIP-UP SUNGLASSES W/POLORIZED LENS?
MODEL F 1 FLIP-UP SUNGLASSES W/POLORIZED LENS is a medical device that received FDA 510(k) clearance on 1990-05-03. The listed applicant is J & B Assoc.. The 510(k) number is K900526.
When did MODEL F 1 FLIP-UP SUNGLASSES W/POLORIZED LENS receive FDA 510(k) clearance?
MODEL F 1 FLIP-UP SUNGLASSES W/POLORIZED LENS received FDA 510(k) clearance on 1990-05-03, under 510(k) number K900526.
Who is the listed applicant for MODEL F 1 FLIP-UP SUNGLASSES W/POLORIZED LENS?
The FDA 510(k) record lists J & B Assoc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL F 1 FLIP-UP SUNGLASSES W/POLORIZED LENS?
The FDA product code for MODEL F 1 FLIP-UP SUNGLASSES W/POLORIZED LENS 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 J & B Assoc. 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.
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