FDA 510(k)

JMS NEEDLES & JMS SYRINGES

K-Number: K845043 · 1985-04-29

Decision Date1985-04-29

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

JMS NEEDLES & JMS SYRINGES 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 1985-04-29 under 510(k) number K845043. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JMS NEEDLES & JMS SYRINGES?

JMS NEEDLES & JMS SYRINGES is a medical device that received FDA 510(k) clearance on 1985-04-29. The listed applicant is Jms Co., Ltd.. The 510(k) number is K845043.

When did JMS NEEDLES & JMS SYRINGES receive FDA 510(k) clearance?

JMS NEEDLES & JMS SYRINGES received FDA 510(k) clearance on 1985-04-29, under 510(k) number K845043.

Who is the listed applicant for JMS NEEDLES & JMS SYRINGES?

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 NEEDLES & JMS SYRINGES?

The FDA product code for JMS NEEDLES & JMS SYRINGES is FMI.

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

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Related Devices (Code: FMI)

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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.