EAGLE VISION-FREEMAN(TM) PUNCTAL VALVE
K-Number: K890920 · 1989-04-11
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Device Summary
Frequently Asked Questions
What is the EAGLE VISION-FREEMAN(TM) PUNCTAL VALVE?
EAGLE VISION-FREEMAN(TM) PUNCTAL VALVE is a medical device that received FDA 510(k) clearance on 1989-04-11. The listed applicant is Eagle Vision, Inc.. The 510(k) number is K890920.
When did EAGLE VISION-FREEMAN(TM) PUNCTAL VALVE receive FDA 510(k) clearance?
EAGLE VISION-FREEMAN(TM) PUNCTAL VALVE received FDA 510(k) clearance on 1989-04-11, under 510(k) number K890920.
Who is the listed applicant for EAGLE VISION-FREEMAN(TM) PUNCTAL VALVE?
The FDA 510(k) record lists Eagle Vision, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EAGLE VISION-FREEMAN(TM) PUNCTAL VALVE?
The FDA product code for EAGLE VISION-FREEMAN(TM) PUNCTAL VALVE is LZU.
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 Eagle Vision, 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: LZU)
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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