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FDA 510(k)

REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER

K-Number: K934727 · 1994-01-10

ApplicantCardiac Pacemakers, Inc.
Decision Date1994-01-10
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER is the device name listed in this FDA 510(k) record. The listed applicant is Cardiac Pacemakers, Inc.. It received FDA 510(k) clearance on 1994-01-10 under 510(k) number K934727. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER?

REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER is a medical device that received FDA 510(k) clearance on 1994-01-10. The listed applicant is Cardiac Pacemakers, Inc.. The 510(k) number is K934727.

When did REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER receive FDA 510(k) clearance?

REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER received FDA 510(k) clearance on 1994-01-10, under 510(k) number K934727.

Who is the listed applicant for REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER?

The FDA 510(k) record lists Cardiac Pacemakers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER?

The FDA product code for REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER is DWS.

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Related Devices (Code: DWS)

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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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