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FDA 510(k)

OXYMIZER-PENDANT

K-Number: K834588 · 1984-03-19

ApplicantChad Therapeutics, Inc.
Decision Date1984-03-19
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYMIZER-PENDANT 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 1984-03-19 under 510(k) number K834588. 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 OXYMIZER-PENDANT?

OXYMIZER-PENDANT is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is Chad Therapeutics, Inc.. The 510(k) number is K834588.

When did OXYMIZER-PENDANT receive FDA 510(k) clearance?

OXYMIZER-PENDANT received FDA 510(k) clearance on 1984-03-19, under 510(k) number K834588.

Who is the listed applicant for OXYMIZER-PENDANT?

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 OXYMIZER-PENDANT?

The FDA product code for OXYMIZER-PENDANT is NFB.

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Other records listing Chad Therapeutics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: 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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