Decision Date1994-02-18
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
CONMED ECG PATIENT CABLES AND LEADWIRES is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1994-02-18 under 510(k) number K933649. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CONMED ECG PATIENT CABLES AND LEADWIRES?
CONMED ECG PATIENT CABLES AND LEADWIRES is a medical device that received FDA 510(k) clearance on 1994-02-18. The listed applicant is Conmedcorp. The 510(k) number is K933649.
When did CONMED ECG PATIENT CABLES AND LEADWIRES receive FDA 510(k) clearance?
CONMED ECG PATIENT CABLES AND LEADWIRES received FDA 510(k) clearance on 1994-02-18, under 510(k) number K933649.
Who is the listed applicant for CONMED ECG PATIENT CABLES AND LEADWIRES?
The FDA 510(k) record lists Conmedcorp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONMED ECG PATIENT CABLES AND LEADWIRES?
The FDA product code for CONMED ECG PATIENT CABLES AND LEADWIRES is DSA.
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Official Source
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