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FDA 510(k)

MYOWIRE-ATEMPORARY CARDIAC PACING WIRE

K-Number: K803086 · 1981-07-01

Decision Date1981-07-01
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MYOWIRE-ATEMPORARY CARDIAC PACING WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Craig & Craig, Inc.. It received FDA 510(k) clearance on 1981-07-01 under 510(k) number K803086. 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 MYOWIRE-ATEMPORARY CARDIAC PACING WIRE?

MYOWIRE-ATEMPORARY CARDIAC PACING WIRE is a medical device that received FDA 510(k) clearance on 1981-07-01. The listed applicant is Craig & Craig, Inc.. The 510(k) number is K803086.

When did MYOWIRE-ATEMPORARY CARDIAC PACING WIRE receive FDA 510(k) clearance?

MYOWIRE-ATEMPORARY CARDIAC PACING WIRE received FDA 510(k) clearance on 1981-07-01, under 510(k) number K803086.

Who is the listed applicant for MYOWIRE-ATEMPORARY CARDIAC PACING WIRE?

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

What is the FDA product code for MYOWIRE-ATEMPORARY CARDIAC PACING WIRE?

The FDA product code for MYOWIRE-ATEMPORARY 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.

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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