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FDA 510(k)

FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT

K-Number: K855139 · 1986-02-26

Decision Date1986-02-26
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1986-02-26 under 510(k) number K855139. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT?

FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT is a medical device that received FDA 510(k) clearance on 1986-02-26. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K855139.

When did FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT receive FDA 510(k) clearance?

FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT received FDA 510(k) clearance on 1986-02-26, under 510(k) number K855139.

Who is the listed applicant for FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT?

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

What is the FDA product code for FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT?

The FDA product code for FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT is LDF.

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 Davis & Geck, 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 45 devices →

Related Devices (Code: LDF)

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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