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FDA 510(k)

AG-839PA CO2 MODULE AND ACCESSORIES

K-Number: K944027 · 1994-08-31

ApplicantNihon Kohden America, Inc.
Decision Date1994-08-31
Product CodeBXO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AG-839PA CO2 MODULE 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 1994-08-31 under 510(k) number K944027. The device is classified under product code BXO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AG-839PA CO2 MODULE AND ACCESSORIES?

AG-839PA CO2 MODULE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-08-31. The listed applicant is Nihon Kohden America, Inc.. The 510(k) number is K944027.

When did AG-839PA CO2 MODULE AND ACCESSORIES receive FDA 510(k) clearance?

AG-839PA CO2 MODULE AND ACCESSORIES received FDA 510(k) clearance on 1994-08-31, under 510(k) number K944027.

Who is the listed applicant for AG-839PA CO2 MODULE 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 AG-839PA CO2 MODULE AND ACCESSORIES?

The FDA product code for AG-839PA CO2 MODULE AND ACCESSORIES is BXO.

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Other records listing Nihon Kohden America, Inc. as applicant

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Related Devices (Code: BXO)

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.

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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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