LEM SPECTACLE FRAMES DIFFERENT COLORS AND DESIGNS
K-Number: K870220 · 1987-04-16
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Device Summary
Frequently Asked Questions
What is the LEM SPECTACLE FRAMES DIFFERENT COLORS AND DESIGNS?
LEM SPECTACLE FRAMES DIFFERENT COLORS AND DESIGNS is a medical device that received FDA 510(k) clearance on 1987-04-16. The listed applicant is Lem Srl.. The 510(k) number is K870220.
When did LEM SPECTACLE FRAMES DIFFERENT COLORS AND DESIGNS receive FDA 510(k) clearance?
LEM SPECTACLE FRAMES DIFFERENT COLORS AND DESIGNS received FDA 510(k) clearance on 1987-04-16, under 510(k) number K870220.
Who is the listed applicant for LEM SPECTACLE FRAMES DIFFERENT COLORS AND DESIGNS?
The FDA 510(k) record lists Lem Srl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEM SPECTACLE FRAMES DIFFERENT COLORS AND DESIGNS?
The FDA product code for LEM SPECTACLE FRAMES DIFFERENT COLORS AND DESIGNS 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 Lem Srl. 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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