FDA 510(k)

MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE

K-Number: K893633 · 1989-06-20

Decision Date1989-06-20

Product CodeDTE

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1989-06-20 under 510(k) number K893633. The device is classified under product code DTE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE?

MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE is a medical device that received FDA 510(k) clearance on 1989-06-20. The listed applicant is Medtronic Vascular. The 510(k) number is K893633.

When did MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE receive FDA 510(k) clearance?

MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE received FDA 510(k) clearance on 1989-06-20, under 510(k) number K893633.

Who is the listed applicant for MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE?

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 MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE?

The FDA product code for MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE is DTE.

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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.