SPECTACLE FRAME
K-Number: K930331 · 1993-12-08
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Device Summary
Frequently Asked Questions
What is the SPECTACLE FRAME?
SPECTACLE FRAME is a medical device that received FDA 510(k) clearance on 1993-12-08. The listed applicant is Australian Optical Co., Inc.. The 510(k) number is K930331.
When did SPECTACLE FRAME receive FDA 510(k) clearance?
SPECTACLE FRAME received FDA 510(k) clearance on 1993-12-08, under 510(k) number K930331.
Who is the listed applicant for SPECTACLE FRAME?
The FDA 510(k) record lists Australian Optical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPECTACLE FRAME?
The FDA product code for SPECTACLE 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 Australian 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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