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FDA 510(k)

EXTERNAL VALVE FUNCTION BLOCK

K-Number: K830914 · 1983-08-12

ApplicantHoneywell, Inc.
Decision Date1983-08-12
Product CodeDRQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EXTERNAL VALVE FUNCTION BLOCK is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K830914. The device is classified under product code DRQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTERNAL VALVE FUNCTION BLOCK?

EXTERNAL VALVE FUNCTION BLOCK is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Honeywell, Inc.. The 510(k) number is K830914.

When did EXTERNAL VALVE FUNCTION BLOCK receive FDA 510(k) clearance?

EXTERNAL VALVE FUNCTION BLOCK received FDA 510(k) clearance on 1983-08-12, under 510(k) number K830914.

Who is the listed applicant for EXTERNAL VALVE FUNCTION BLOCK?

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 EXTERNAL VALVE FUNCTION BLOCK?

The FDA product code for EXTERNAL VALVE FUNCTION BLOCK is DRQ.

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Other records listing Honeywell, Inc. as applicant

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Related Devices (Code: DRQ)

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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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