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FDA 510(k)

EAGLE VISION FREEMAN RADIOPAGUE PUNCTUM PLUG

K-Number: K905427 · 1991-06-06

Decision Date1991-06-06
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

EAGLE VISION FREEMAN RADIOPAGUE PUNCTUM PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Eagle Vision, Inc.. It received FDA 510(k) clearance on 1991-06-06 under 510(k) number K905427. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAGLE VISION FREEMAN RADIOPAGUE PUNCTUM PLUG?

EAGLE VISION FREEMAN RADIOPAGUE PUNCTUM PLUG is a medical device that received FDA 510(k) clearance on 1991-06-06. The listed applicant is Eagle Vision, Inc.. The 510(k) number is K905427.

When did EAGLE VISION FREEMAN RADIOPAGUE PUNCTUM PLUG receive FDA 510(k) clearance?

EAGLE VISION FREEMAN RADIOPAGUE PUNCTUM PLUG received FDA 510(k) clearance on 1991-06-06, under 510(k) number K905427.

Who is the listed applicant for EAGLE VISION FREEMAN RADIOPAGUE PUNCTUM PLUG?

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 RADIOPAGUE PUNCTUM PLUG?

The FDA product code for EAGLE VISION FREEMAN RADIOPAGUE PUNCTUM PLUG 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.

View all 7 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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