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FDA 510(k)

LIFECYCLE AEROBIC MONITOR 123

K-Number: K840488 · 1984-05-30

ApplicantHeart Rate, Inc.
Decision Date1984-05-30
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIFECYCLE AEROBIC MONITOR 123 is the device name listed in this FDA 510(k) record. The listed applicant is Heart Rate, Inc.. It received FDA 510(k) clearance on 1984-05-30 under 510(k) number K840488. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFECYCLE AEROBIC MONITOR 123?

LIFECYCLE AEROBIC MONITOR 123 is a medical device that received FDA 510(k) clearance on 1984-05-30. The listed applicant is Heart Rate, Inc.. The 510(k) number is K840488.

When did LIFECYCLE AEROBIC MONITOR 123 receive FDA 510(k) clearance?

LIFECYCLE AEROBIC MONITOR 123 received FDA 510(k) clearance on 1984-05-30, under 510(k) number K840488.

Who is the listed applicant for LIFECYCLE AEROBIC MONITOR 123?

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

What is the FDA product code for LIFECYCLE AEROBIC MONITOR 123?

The FDA product code for LIFECYCLE AEROBIC MONITOR 123 is BZQ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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