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FDA 510(k)

POST EXTRA SYSTOLIC POSTENTLATOR

K-Number: K791959 · 1980-01-09

ApplicantMedrad, Inc.
Decision Date1980-01-09
Product CodeIXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POST EXTRA SYSTOLIC POSTENTLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1980-01-09 under 510(k) number K791959. The device is classified under product code IXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POST EXTRA SYSTOLIC POSTENTLATOR?

POST EXTRA SYSTOLIC POSTENTLATOR is a medical device that received FDA 510(k) clearance on 1980-01-09. The listed applicant is Medrad, Inc.. The 510(k) number is K791959.

When did POST EXTRA SYSTOLIC POSTENTLATOR receive FDA 510(k) clearance?

POST EXTRA SYSTOLIC POSTENTLATOR received FDA 510(k) clearance on 1980-01-09, under 510(k) number K791959.

Who is the listed applicant for POST EXTRA SYSTOLIC POSTENTLATOR?

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

What is the FDA product code for POST EXTRA SYSTOLIC POSTENTLATOR?

The FDA product code for POST EXTRA SYSTOLIC POSTENTLATOR is IXO.

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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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