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FDA 510(k)

DEKNATEL TEMPORARY CARDIAC PACING WIRE

K-Number: K873728 · 1987-11-03

Decision Date1987-11-03
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DEKNATEL TEMPORARY CARDIAC PACING WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Deknatel, Inc.. It received FDA 510(k) clearance on 1987-11-03 under 510(k) number K873728. 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 DEKNATEL TEMPORARY CARDIAC PACING WIRE?

DEKNATEL TEMPORARY CARDIAC PACING WIRE is a medical device that received FDA 510(k) clearance on 1987-11-03. The listed applicant is Deknatel, Inc.. The 510(k) number is K873728.

When did DEKNATEL TEMPORARY CARDIAC PACING WIRE receive FDA 510(k) clearance?

DEKNATEL TEMPORARY CARDIAC PACING WIRE received FDA 510(k) clearance on 1987-11-03, under 510(k) number K873728.

Who is the listed applicant for DEKNATEL TEMPORARY CARDIAC PACING WIRE?

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

What is the FDA product code for DEKNATEL TEMPORARY CARDIAC PACING WIRE?

The FDA product code for DEKNATEL TEMPORARY CARDIAC PACING WIRE 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 Deknatel, 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 37 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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