EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS
K-Number: K941052 · 1994-04-12
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Device Summary
Frequently Asked Questions
What is the EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS?
EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS is a medical device that received FDA 510(k) clearance on 1994-04-12. The listed applicant is Atlantic Optical Co., Inc.. The 510(k) number is K941052.
When did EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS receive FDA 510(k) clearance?
EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS received FDA 510(k) clearance on 1994-04-12, under 510(k) number K941052.
Who is the listed applicant for EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS?
The FDA 510(k) record lists Atlantic Optical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS?
The FDA product code for EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS is HQZ.
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 Atlantic Optical 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: HQZ)
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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