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FDA 510(k)

CARDIORATER CR-3

K-Number: K812145 · 1981-09-25

ApplicantLife Science Instrumentation, Inc.
Decision Date1981-09-25
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIORATER CR-3 is the device name listed in this FDA 510(k) record. The listed applicant is Life Science Instrumentation, Inc.. It received FDA 510(k) clearance on 1981-09-25 under 510(k) number K812145. 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 CARDIORATER CR-3?

CARDIORATER CR-3 is a medical device that received FDA 510(k) clearance on 1981-09-25. The listed applicant is Life Science Instrumentation, Inc.. The 510(k) number is K812145.

When did CARDIORATER CR-3 receive FDA 510(k) clearance?

CARDIORATER CR-3 received FDA 510(k) clearance on 1981-09-25, under 510(k) number K812145.

Who is the listed applicant for CARDIORATER CR-3?

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

What is the FDA product code for CARDIORATER CR-3?

The FDA product code for CARDIORATER CR-3 is DRT.

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Other records listing Life Science Instrumentation, Inc. as applicant

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Related Devices (Code: DRT)

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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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