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FDA 510(k)

THE ABBOTT EXECUTIVE

K-Number: K790543 · 1979-05-03

ApplicantAbbott Laboratories
Decision Date1979-05-03
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

THE ABBOTT EXECUTIVE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1979-05-03 under 510(k) number K790543. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE ABBOTT EXECUTIVE?

THE ABBOTT EXECUTIVE is a medical device that received FDA 510(k) clearance on 1979-05-03. The listed applicant is Abbott Laboratories. The 510(k) number is K790543.

When did THE ABBOTT EXECUTIVE receive FDA 510(k) clearance?

THE ABBOTT EXECUTIVE received FDA 510(k) clearance on 1979-05-03, under 510(k) number K790543.

Who is the listed applicant for THE ABBOTT EXECUTIVE?

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

What is the FDA product code for THE ABBOTT EXECUTIVE?

The FDA product code for THE ABBOTT EXECUTIVE is JQP.

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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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