FOG CONTROL, LENS FOG REDUCTION DEVICE
K-Number: K932300 · 1993-09-17
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Device Summary
Frequently Asked Questions
What is the FOG CONTROL, LENS FOG REDUCTION DEVICE?
FOG CONTROL, LENS FOG REDUCTION DEVICE is a medical device that received FDA 510(k) clearance on 1993-09-17. The listed applicant is Highpoint Medical Corp.. The 510(k) number is K932300.
When did FOG CONTROL, LENS FOG REDUCTION DEVICE receive FDA 510(k) clearance?
FOG CONTROL, LENS FOG REDUCTION DEVICE received FDA 510(k) clearance on 1993-09-17, under 510(k) number K932300.
Who is the listed applicant for FOG CONTROL, LENS FOG REDUCTION DEVICE?
The FDA 510(k) record lists Highpoint Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FOG CONTROL, LENS FOG REDUCTION DEVICE?
The FDA product code for FOG CONTROL, LENS FOG REDUCTION DEVICE is OCT.
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 Highpoint Medical Corp. 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: OCT)
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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