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FDA 510(k)

LIFEWATCH PLUS

K-Number: K870661 · 1987-03-09

ApplicantThe Perkin-Elmer Corp.
Decision Date1987-03-09
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIFEWATCH PLUS is the device name listed in this FDA 510(k) record. The listed applicant is The Perkin-Elmer Corp.. It received FDA 510(k) clearance on 1987-03-09 under 510(k) number K870661. 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 LIFEWATCH PLUS?

LIFEWATCH PLUS is a medical device that received FDA 510(k) clearance on 1987-03-09. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K870661.

When did LIFEWATCH PLUS receive FDA 510(k) clearance?

LIFEWATCH PLUS received FDA 510(k) clearance on 1987-03-09, under 510(k) number K870661.

Who is the listed applicant for LIFEWATCH PLUS?

The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFEWATCH PLUS?

The FDA product code for LIFEWATCH PLUS is BZQ.

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Other records listing The Perkin-Elmer Corp. as applicant

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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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