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FDA 510(k)

NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION

K-Number: K102106 · 2010-12-17

ApplicantNihon Kohden Corp.
Decision Date2010-12-17
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden Corp.. It received FDA 510(k) clearance on 2010-12-17 under 510(k) number K102106. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION?

NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION is a medical device that received FDA 510(k) clearance on 2010-12-17. The listed applicant is Nihon Kohden Corp.. The 510(k) number is K102106.

When did NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION receive FDA 510(k) clearance?

NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION received FDA 510(k) clearance on 2010-12-17, under 510(k) number K102106.

Who is the listed applicant for NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION?

The FDA 510(k) record lists Nihon Kohden Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION?

The FDA product code for NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION is DRG.

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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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