WINK-EASE PERSONAL PROTECTIVE EYEWEAR
K-Number: K873662 · 1987-10-02
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Device Summary
Frequently Asked Questions
What is the WINK-EASE PERSONAL PROTECTIVE EYEWEAR?
WINK-EASE PERSONAL PROTECTIVE EYEWEAR is a medical device that received FDA 510(k) clearance on 1987-10-02. The listed applicant is Eye Pro Medical Products, Inc.. The 510(k) number is K873662.
When did WINK-EASE PERSONAL PROTECTIVE EYEWEAR receive FDA 510(k) clearance?
WINK-EASE PERSONAL PROTECTIVE EYEWEAR received FDA 510(k) clearance on 1987-10-02, under 510(k) number K873662.
Who is the listed applicant for WINK-EASE PERSONAL PROTECTIVE EYEWEAR?
The FDA 510(k) record lists Eye Pro Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WINK-EASE PERSONAL PROTECTIVE EYEWEAR?
The FDA product code for WINK-EASE PERSONAL PROTECTIVE EYEWEAR is HOY.
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 Eye Pro Medical Products, 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: HOY)
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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