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FDA 510(k)

A-V IMPULSE SYSTEM MODEL 6060

K-Number: K964425 · 1997-07-28

ApplicantPowell,Goldstein,Frazer & Murphy
Decision Date1997-07-28
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

A-V IMPULSE SYSTEM MODEL 6060 is the device name listed in this FDA 510(k) record. The listed applicant is Powell,Goldstein,Frazer & Murphy. It received FDA 510(k) clearance on 1997-07-28 under 510(k) number K964425. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-V IMPULSE SYSTEM MODEL 6060?

A-V IMPULSE SYSTEM MODEL 6060 is a medical device that received FDA 510(k) clearance on 1997-07-28. The listed applicant is Powell,Goldstein,Frazer & Murphy. The 510(k) number is K964425.

When did A-V IMPULSE SYSTEM MODEL 6060 receive FDA 510(k) clearance?

A-V IMPULSE SYSTEM MODEL 6060 received FDA 510(k) clearance on 1997-07-28, under 510(k) number K964425.

Who is the listed applicant for A-V IMPULSE SYSTEM MODEL 6060?

The FDA 510(k) record lists Powell,Goldstein,Frazer & Murphy as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A-V IMPULSE SYSTEM MODEL 6060?

The FDA product code for A-V IMPULSE SYSTEM MODEL 6060 is JOW.

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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.

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