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FDA 510(k)

CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S

K-Number: K042142 · 2004-09-20

ApplicantChad Therapeutics, Inc.
Decision Date2004-09-20
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S is the device name listed in this FDA 510(k) record. The listed applicant is Chad Therapeutics, Inc.. It received FDA 510(k) clearance on 2004-09-20 under 510(k) number K042142. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S?

CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S is a medical device that received FDA 510(k) clearance on 2004-09-20. The listed applicant is Chad Therapeutics, Inc.. The 510(k) number is K042142.

When did CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S receive FDA 510(k) clearance?

CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S received FDA 510(k) clearance on 2004-09-20, under 510(k) number K042142.

Who is the listed applicant for CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S?

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

What is the FDA product code for CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S?

The FDA product code for CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S is NFB.

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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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