MYOWIRE-ATEMPORARY CARDIAC PACING WIRE
K-Number: K803086 · 1981-07-01
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Device Summary
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
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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