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FDA 510(k)

OSCILLAIRE

K-Number: K812001 · 1981-08-20

ApplicantJones Medical Instrument Co.
Decision Date1981-08-20
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OSCILLAIRE is the device name listed in this FDA 510(k) record. The listed applicant is Jones Medical Instrument Co.. It received FDA 510(k) clearance on 1981-08-20 under 510(k) number K812001. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSCILLAIRE?

OSCILLAIRE is a medical device that received FDA 510(k) clearance on 1981-08-20. The listed applicant is Jones Medical Instrument Co.. The 510(k) number is K812001.

When did OSCILLAIRE receive FDA 510(k) clearance?

OSCILLAIRE received FDA 510(k) clearance on 1981-08-20, under 510(k) number K812001.

Who is the listed applicant for OSCILLAIRE?

The FDA 510(k) record lists Jones Medical Instrument Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSCILLAIRE?

The FDA product code for OSCILLAIRE is BZC.

Related Clinical Trials

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Other records listing Jones Medical Instrument Co. 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.

K771147AVL BLOOD GAS INSTRUMENT MODEL 939

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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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