ARTSUN OPTICAL FRAME
K-Number: K940782 · 1994-04-12
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Device Summary
Frequently Asked Questions
What is the ARTSUN OPTICAL FRAME?
ARTSUN OPTICAL FRAME is a medical device that received FDA 510(k) clearance on 1994-04-12. The listed applicant is Frontier Novelty, Inc.. The 510(k) number is K940782.
When did ARTSUN OPTICAL FRAME receive FDA 510(k) clearance?
ARTSUN OPTICAL FRAME received FDA 510(k) clearance on 1994-04-12, under 510(k) number K940782.
Who is the listed applicant for ARTSUN OPTICAL FRAME?
The FDA 510(k) record lists Frontier Novelty, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTSUN OPTICAL FRAME?
The FDA product code for ARTSUN OPTICAL FRAME 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 Frontier Novelty, 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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