Decision Date1981-10-29
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
TEMPORARY PERVENOUS J-ATRIAL LEAD is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1981-10-29 under 510(k) number K812781. 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 TEMPORARY PERVENOUS J-ATRIAL LEAD?
TEMPORARY PERVENOUS J-ATRIAL LEAD is a medical device that received FDA 510(k) clearance on 1981-10-29. The listed applicant is Cordis Corp.. The 510(k) number is K812781.
When did TEMPORARY PERVENOUS J-ATRIAL LEAD receive FDA 510(k) clearance?
TEMPORARY PERVENOUS J-ATRIAL LEAD received FDA 510(k) clearance on 1981-10-29, under 510(k) number K812781.
Who is the listed applicant for TEMPORARY PERVENOUS J-ATRIAL LEAD?
The FDA 510(k) record lists Cordis Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TEMPORARY PERVENOUS J-ATRIAL LEAD?
The FDA product code for TEMPORARY PERVENOUS J-ATRIAL LEAD is LDF.
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Official Source
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