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FDA 510(k)

FLEXPLUG

K-Number: K991130 · 1999-04-20

Decision Date1999-04-20
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

FLEXPLUG 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 1999-04-20 under 510(k) number K991130. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXPLUG?

FLEXPLUG is a medical device that received FDA 510(k) clearance on 1999-04-20. The listed applicant is Eagle Vision, Inc.. The 510(k) number is K991130.

When did FLEXPLUG receive FDA 510(k) clearance?

FLEXPLUG received FDA 510(k) clearance on 1999-04-20, under 510(k) number K991130.

Who is the listed applicant for FLEXPLUG?

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 FLEXPLUG?

The FDA product code for FLEXPLUG 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

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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