SUNGLASSES (NON-PERSCRIPTION)
K-Number: K934567 · 1994-03-24
Device Summary
Frequently Asked Questions
What is the SUNGLASSES (NON-PERSCRIPTION)?
SUNGLASSES (NON-PERSCRIPTION) is a medical device that received FDA 510(k) clearance on 1994-03-24. The listed applicant is Jaan Huey Co., Ltd.. The 510(k) number is K934567.
When did SUNGLASSES (NON-PERSCRIPTION) receive FDA 510(k) clearance?
SUNGLASSES (NON-PERSCRIPTION) received FDA 510(k) clearance on 1994-03-24, under 510(k) number K934567.
Who is the listed applicant for SUNGLASSES (NON-PERSCRIPTION)?
The FDA 510(k) record lists Jaan Huey Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUNGLASSES (NON-PERSCRIPTION)?
The FDA product code for SUNGLASSES (NON-PERSCRIPTION) 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.