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FDA 510(k)

PRESSURE MANOMETER

K-Number: K841071 · 1984-04-17

ApplicantInterventional Medical, Inc.
Decision Date1984-04-17
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRESSURE MANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Interventional Medical, Inc.. It received FDA 510(k) clearance on 1984-04-17 under 510(k) number K841071. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE MANOMETER?

PRESSURE MANOMETER is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Interventional Medical, Inc.. The 510(k) number is K841071.

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

PRESSURE MANOMETER received FDA 510(k) clearance on 1984-04-17, under 510(k) number K841071.

Who is the listed applicant for PRESSURE MANOMETER?

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

What is the FDA product code for PRESSURE MANOMETER?

The FDA product code for PRESSURE MANOMETER is DQX.

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Other records listing Interventional Medical, Inc. as applicant

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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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