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FDA 510(k)

PRESSURE FUNCTION BLOCK FOR BLOOD PRESS

K-Number: K830779 · 1983-05-09

ApplicantHoneywell, Inc.
Decision Date1983-05-09
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRESSURE FUNCTION BLOCK FOR BLOOD PRESS is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K830779. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE FUNCTION BLOCK FOR BLOOD PRESS?

PRESSURE FUNCTION BLOCK FOR BLOOD PRESS is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Honeywell, Inc.. The 510(k) number is K830779.

When did PRESSURE FUNCTION BLOCK FOR BLOOD PRESS receive FDA 510(k) clearance?

PRESSURE FUNCTION BLOCK FOR BLOOD PRESS received FDA 510(k) clearance on 1983-05-09, under 510(k) number K830779.

Who is the listed applicant for PRESSURE FUNCTION BLOCK FOR BLOOD PRESS?

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

What is the FDA product code for PRESSURE FUNCTION BLOCK FOR BLOOD PRESS?

The FDA product code for PRESSURE FUNCTION BLOCK FOR BLOOD PRESS is DRT.

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Other records listing Honeywell, 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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