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FDA 510(k)

JLS GROUP INFANT MONITOR

K-Number: K820374 · 1982-03-26

ApplicantJls Group, Inc.
Decision Date1982-03-26
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

JLS GROUP INFANT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Jls Group, Inc.. It received FDA 510(k) clearance on 1982-03-26 under 510(k) number K820374. 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 JLS GROUP INFANT MONITOR?

JLS GROUP INFANT MONITOR is a medical device that received FDA 510(k) clearance on 1982-03-26. The listed applicant is Jls Group, Inc.. The 510(k) number is K820374.

When did JLS GROUP INFANT MONITOR receive FDA 510(k) clearance?

JLS GROUP INFANT MONITOR received FDA 510(k) clearance on 1982-03-26, under 510(k) number K820374.

Who is the listed applicant for JLS GROUP INFANT MONITOR?

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

What is the FDA product code for JLS GROUP INFANT MONITOR?

The FDA product code for JLS GROUP INFANT MONITOR 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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