Decision Date1983-10-19
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
EPCOR MULTIELECTRODE TEMP. PERVENOUS is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1983-10-19 under 510(k) number K832561. 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 EPCOR MULTIELECTRODE TEMP. PERVENOUS?
EPCOR MULTIELECTRODE TEMP. PERVENOUS is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Cordis Corp.. The 510(k) number is K832561.
When did EPCOR MULTIELECTRODE TEMP. PERVENOUS receive FDA 510(k) clearance?
EPCOR MULTIELECTRODE TEMP. PERVENOUS received FDA 510(k) clearance on 1983-10-19, under 510(k) number K832561.
Who is the listed applicant for EPCOR MULTIELECTRODE TEMP. PERVENOUS?
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 EPCOR MULTIELECTRODE TEMP. PERVENOUS?
The FDA product code for EPCOR MULTIELECTRODE TEMP. PERVENOUS is LDF.
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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.