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FDA 510(k)

MODEL K110SX CENTRIFUGE

K-Number: K861146 · 1986-05-05

ApplicantJouan S.A.
Decision Date1986-05-05
Product CodeJQC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODEL K110SX CENTRIFUGE is the device name listed in this FDA 510(k) record. The listed applicant is Jouan S.A.. It received FDA 510(k) clearance on 1986-05-05 under 510(k) number K861146. The device is classified under product code JQC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL K110SX CENTRIFUGE?

MODEL K110SX CENTRIFUGE is a medical device that received FDA 510(k) clearance on 1986-05-05. The listed applicant is Jouan S.A.. The 510(k) number is K861146.

When did MODEL K110SX CENTRIFUGE receive FDA 510(k) clearance?

MODEL K110SX CENTRIFUGE received FDA 510(k) clearance on 1986-05-05, under 510(k) number K861146.

Who is the listed applicant for MODEL K110SX CENTRIFUGE?

The FDA 510(k) record lists Jouan S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL K110SX CENTRIFUGE?

The FDA product code for MODEL K110SX CENTRIFUGE is JQC.

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Related Devices (Code: JQC)

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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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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