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FDA 510(k)

IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS)

K-Number: K924360 · 1992-11-25

ApplicantImpra, Inc.
Decision Date1992-11-25
Product CodeDYF
Advisory CommitteeCV
DecisionUnknown

Device Summary

IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS) is the device name listed in this FDA 510(k) record. The listed applicant is Impra, Inc.. It received FDA 510(k) clearance on 1992-11-25 under 510(k) number K924360. The device is classified under product code DYF. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS)?

IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS) is a medical device that received FDA 510(k) clearance on 1992-11-25. The listed applicant is Impra, Inc.. The 510(k) number is K924360.

When did IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS) receive FDA 510(k) clearance?

IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS) received FDA 510(k) clearance on 1992-11-25, under 510(k) number K924360.

Who is the listed applicant for IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS)?

The FDA 510(k) record lists Impra, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS)?

The FDA product code for IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS) is DYF.

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 Impra, 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.

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Related Devices (Code: DYF)

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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