MULTIPLE SPECTACLE FRAMES
K-Number: K883100 · 1988-08-25
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Device Summary
Frequently Asked Questions
What is the MULTIPLE SPECTACLE FRAMES?
MULTIPLE SPECTACLE FRAMES is a medical device that received FDA 510(k) clearance on 1988-08-25. The listed applicant is Metal Optics U.S.A., Inc.. The 510(k) number is K883100.
When did MULTIPLE SPECTACLE FRAMES receive FDA 510(k) clearance?
MULTIPLE SPECTACLE FRAMES received FDA 510(k) clearance on 1988-08-25, under 510(k) number K883100.
Who is the listed applicant for MULTIPLE SPECTACLE FRAMES?
The FDA 510(k) record lists Metal Optics U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTIPLE SPECTACLE FRAMES?
The FDA product code for MULTIPLE SPECTACLE FRAMES 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.
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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