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FDA 510(k)

HUMIDIFIERS, MODEL:LS-420 AND LS-460

K-Number: K781760 · 1978-12-20

ApplicantBourns Medical Systems, Inc.
Decision Date1978-12-20
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HUMIDIFIERS, MODEL:LS-420 AND LS-460 is the device name listed in this FDA 510(k) record. The listed applicant is Bourns Medical Systems, Inc.. It received FDA 510(k) clearance on 1978-12-20 under 510(k) number K781760. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMIDIFIERS, MODEL:LS-420 AND LS-460?

HUMIDIFIERS, MODEL:LS-420 AND LS-460 is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is Bourns Medical Systems, Inc.. The 510(k) number is K781760.

When did HUMIDIFIERS, MODEL:LS-420 AND LS-460 receive FDA 510(k) clearance?

HUMIDIFIERS, MODEL:LS-420 AND LS-460 received FDA 510(k) clearance on 1978-12-20, under 510(k) number K781760.

Who is the listed applicant for HUMIDIFIERS, MODEL:LS-420 AND LS-460?

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

What is the FDA product code for HUMIDIFIERS, MODEL:LS-420 AND LS-460?

The FDA product code for HUMIDIFIERS, MODEL:LS-420 AND LS-460 is BTT.

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Other records listing Bourns Medical Systems, Inc. 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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