SUNGLASSES
K-Number: K902343 · 1991-02-26
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Device Summary
Frequently Asked Questions
What is the SUNGLASSES?
SUNGLASSES is a medical device that received FDA 510(k) clearance on 1991-02-26. The listed applicant is Jasco Products Co., Inc.. The 510(k) number is K902343.
When did SUNGLASSES receive FDA 510(k) clearance?
SUNGLASSES received FDA 510(k) clearance on 1991-02-26, under 510(k) number K902343.
Who is the listed applicant for SUNGLASSES?
The FDA 510(k) record lists Jasco Products Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUNGLASSES?
The FDA product code for 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.
Other records listing Jasco Products Co., 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: 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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