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FDA 510(k)

CONMED EKG STRIPPER

K-Number: K960264 · 1996-04-09

ApplicantConmedcorp
Decision Date1996-04-09
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONMED EKG STRIPPER is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1996-04-09 under 510(k) number K960264. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONMED EKG STRIPPER?

CONMED EKG STRIPPER is a medical device that received FDA 510(k) clearance on 1996-04-09. The listed applicant is Conmedcorp. The 510(k) number is K960264.

When did CONMED EKG STRIPPER receive FDA 510(k) clearance?

CONMED EKG STRIPPER received FDA 510(k) clearance on 1996-04-09, under 510(k) number K960264.

Who is the listed applicant for CONMED EKG STRIPPER?

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 EKG STRIPPER?

The FDA product code for CONMED EKG STRIPPER is DRX.

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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.

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