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FDA 510(k)

Nunchaku

K-Number: K161373 · 2016-11-03

ApplicantFci (France Chirurgie Instrumentation)
Decision Date2016-11-03
Product CodeOKS
DecisionSubstantially Equivalent

Device Summary

Nunchaku is the device name listed in this FDA 510(k) record. The listed applicant is Fci (France Chirurgie Instrumentation). It received FDA 510(k) clearance on 2016-11-03 under 510(k) number K161373. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nunchaku?

Nunchaku is a medical device that received FDA 510(k) clearance on 2016-11-03. The listed applicant is Fci (France Chirurgie Instrumentation). The 510(k) number is K161373.

When did Nunchaku receive FDA 510(k) clearance?

Nunchaku received FDA 510(k) clearance on 2016-11-03, under 510(k) number K161373.

Who is the listed applicant for Nunchaku?

The FDA 510(k) record lists Fci (France Chirurgie Instrumentation) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nunchaku?

The FDA product code for Nunchaku is OKS.

Related Devices (Code: OKS)

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.

K201892Ritleng®+ and Ritleng®+ PVPFci (France Chirurgie Instrumentation) SasK201606LacriJet®Fci (France Chirurgie Instrumentation) SasK170247Lacriflow CLKaneka Pharma America, LLCK160710Oasis Lacrimal Intubation SetAnodyne

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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