FDA 510(k)

ALTERNATE PACKAGING CONF. OF PACEMAKER LEAD ADAP.

K-Number: K894976 · 1989-10-12

Decision Date1989-10-12

Product CodeDTD

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ALTERNATE PACKAGING CONF. OF PACEMAKER LEAD ADAP. is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1989-10-12 under 510(k) number K894976. The device is classified under product code DTD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALTERNATE PACKAGING CONF. OF PACEMAKER LEAD ADAP.?

ALTERNATE PACKAGING CONF. OF PACEMAKER LEAD ADAP. is a medical device that received FDA 510(k) clearance on 1989-10-12. The listed applicant is Medtronic Vascular. The 510(k) number is K894976.

When did ALTERNATE PACKAGING CONF. OF PACEMAKER LEAD ADAP. receive FDA 510(k) clearance?

ALTERNATE PACKAGING CONF. OF PACEMAKER LEAD ADAP. received FDA 510(k) clearance on 1989-10-12, under 510(k) number K894976.

Who is the listed applicant for ALTERNATE PACKAGING CONF. OF PACEMAKER LEAD ADAP.?

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 ALTERNATE PACKAGING CONF. OF PACEMAKER LEAD ADAP.?

The FDA product code for ALTERNATE PACKAGING CONF. OF PACEMAKER LEAD ADAP. is DTD.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.