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FDA 510(k)

ARRHYTHMIA FUNCTION BLOCK

K-Number: K811581 · 1981-08-13

ApplicantHoneywell, Inc.
Decision Date1981-08-13
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARRHYTHMIA 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 1981-08-13 under 510(k) number K811581. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARRHYTHMIA FUNCTION BLOCK?

ARRHYTHMIA FUNCTION BLOCK is a medical device that received FDA 510(k) clearance on 1981-08-13. The listed applicant is Honeywell, Inc.. The 510(k) number is K811581.

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

ARRHYTHMIA FUNCTION BLOCK received FDA 510(k) clearance on 1981-08-13, under 510(k) number K811581.

Who is the listed applicant for ARRHYTHMIA 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 ARRHYTHMIA FUNCTION BLOCK?

The FDA product code for ARRHYTHMIA FUNCTION BLOCK is DSI.

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Other records listing Honeywell, Inc. as applicant

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Related Devices (Code: DSI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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