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FDA 510(k)

NIHON KOHDEN OGS-2001A POCKETCARE AND ACCESSORIES

K-Number: K992455 · 2000-01-07

ApplicantNihon Kohden America, Inc.
Decision Date2000-01-07
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NIHON KOHDEN OGS-2001A POCKETCARE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden America, Inc.. It received FDA 510(k) clearance on 2000-01-07 under 510(k) number K992455. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIHON KOHDEN OGS-2001A POCKETCARE AND ACCESSORIES?

NIHON KOHDEN OGS-2001A POCKETCARE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2000-01-07. The listed applicant is Nihon Kohden America, Inc.. The 510(k) number is K992455.

When did NIHON KOHDEN OGS-2001A POCKETCARE AND ACCESSORIES receive FDA 510(k) clearance?

NIHON KOHDEN OGS-2001A POCKETCARE AND ACCESSORIES received FDA 510(k) clearance on 2000-01-07, under 510(k) number K992455.

Who is the listed applicant for NIHON KOHDEN OGS-2001A POCKETCARE AND ACCESSORIES?

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

What is the FDA product code for NIHON KOHDEN OGS-2001A POCKETCARE AND ACCESSORIES?

The FDA product code for NIHON KOHDEN OGS-2001A POCKETCARE AND ACCESSORIES is DQA.

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Other records listing Nihon Kohden America, Inc. as applicant

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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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