SUNGLASS CLIP
K-Number: K943640 · 1994-09-14
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Device Summary
Frequently Asked Questions
What is the SUNGLASS CLIP?
SUNGLASS CLIP is a medical device that received FDA 510(k) clearance on 1994-09-14. The listed applicant is Australian Optical Co., Inc.. The 510(k) number is K943640.
When did SUNGLASS CLIP receive FDA 510(k) clearance?
SUNGLASS CLIP received FDA 510(k) clearance on 1994-09-14, under 510(k) number K943640.
Who is the listed applicant for SUNGLASS CLIP?
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 SUNGLASS CLIP?
The FDA product code for SUNGLASS CLIP is HQY.
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: HQY)
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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