FRAMES, SPECTACLE
K-Number: K932813 · 1993-08-31
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Device Summary
Frequently Asked Questions
What is the FRAMES, SPECTACLE?
FRAMES, SPECTACLE is a medical device that received FDA 510(k) clearance on 1993-08-31. The listed applicant is Rainbow Optics, Inc.. The 510(k) number is K932813.
When did FRAMES, SPECTACLE receive FDA 510(k) clearance?
FRAMES, SPECTACLE received FDA 510(k) clearance on 1993-08-31, under 510(k) number K932813.
Who is the listed applicant for FRAMES, SPECTACLE?
The FDA 510(k) record lists Rainbow Optics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FRAMES, SPECTACLE?
The FDA product code for FRAMES, SPECTACLE 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 Rainbow Optics, 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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