Decision Date1995-12-13
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE MODEL 6494 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1995-12-13 under 510(k) number K954809. 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 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE MODEL 6494?
UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE MODEL 6494 is a medical device that received FDA 510(k) clearance on 1995-12-13. The listed applicant is Medtronic Vascular. The 510(k) number is K954809.
When did UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE MODEL 6494 receive FDA 510(k) clearance?
UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE MODEL 6494 received FDA 510(k) clearance on 1995-12-13, under 510(k) number K954809.
Who is the listed applicant for UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE MODEL 6494?
The FDA 510(k) record lists Medtronic Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE MODEL 6494?
The FDA product code for UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE MODEL 6494 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.