FDA 510(k)

JMS DIALYZER PRIMING SET

K-Number: K895882 · 1990-02-09

Decision Date1990-02-09

Product CodeKOC

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

JMS DIALYZER PRIMING SET is the device name listed in this FDA 510(k) record. The listed applicant is Jms Co., Ltd.. It received FDA 510(k) clearance on 1990-02-09 under 510(k) number K895882. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JMS DIALYZER PRIMING SET?

JMS DIALYZER PRIMING SET is a medical device that received FDA 510(k) clearance on 1990-02-09. The listed applicant is Jms Co., Ltd.. The 510(k) number is K895882.

When did JMS DIALYZER PRIMING SET receive FDA 510(k) clearance?

JMS DIALYZER PRIMING SET received FDA 510(k) clearance on 1990-02-09, under 510(k) number K895882.

Who is the listed applicant for JMS DIALYZER PRIMING SET?

The FDA 510(k) record lists Jms Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JMS DIALYZER PRIMING SET?

The FDA product code for JMS DIALYZER PRIMING SET is KOC.

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Other records listing Jms Co., Ltd. as applicant

K002352JMS A.V. FISTULA NEEDLE SET ACCORDION TYPE K002394JMS APHERESIS NEEDLE SET ACCORDION TYPE K010410JMS APHERESIS NEEDLE WING EATER, MODEL 14G-18G K010406JMS A.V. FISTULA NEEDLE SET WING EATER, MODEL 14G-18G K000843MODIFICATION TO JMS APHERESIS NEEDLE K000845MODIFICATION TO JMS A.V. FISTULA NEEDLE SET

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Related Devices (Code: KOC)

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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.