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FDA 510(k)

POCKET MANOMETER

K-Number: K880599 · 1988-10-06

ApplicantAbbott Laboratories
Decision Date1988-10-06
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

POCKET MANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1988-10-06 under 510(k) number K880599. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POCKET MANOMETER?

POCKET MANOMETER is a medical device that received FDA 510(k) clearance on 1988-10-06. The listed applicant is Abbott Laboratories. The 510(k) number is K880599.

When did POCKET MANOMETER receive FDA 510(k) clearance?

POCKET MANOMETER received FDA 510(k) clearance on 1988-10-06, under 510(k) number K880599.

Who is the listed applicant for POCKET MANOMETER?

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 POCKET MANOMETER?

The FDA product code for POCKET MANOMETER is DXN.

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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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