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FDA 510(k)

MICROPROCESSOR CONTROLLED ELECTROCARDIO

K-Number: K810263 · 1981-02-19

ApplicantHoneywell, Inc.
Decision Date1981-02-19
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROPROCESSOR CONTROLLED ELECTROCARDIO is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1981-02-19 under 510(k) number K810263. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROPROCESSOR CONTROLLED ELECTROCARDIO?

MICROPROCESSOR CONTROLLED ELECTROCARDIO is a medical device that received FDA 510(k) clearance on 1981-02-19. The listed applicant is Honeywell, Inc.. The 510(k) number is K810263.

When did MICROPROCESSOR CONTROLLED ELECTROCARDIO receive FDA 510(k) clearance?

MICROPROCESSOR CONTROLLED ELECTROCARDIO received FDA 510(k) clearance on 1981-02-19, under 510(k) number K810263.

Who is the listed applicant for MICROPROCESSOR CONTROLLED ELECTROCARDIO?

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 MICROPROCESSOR CONTROLLED ELECTROCARDIO?

The FDA product code for MICROPROCESSOR CONTROLLED ELECTROCARDIO is DPS.

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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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