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FDA 510(k)

DMR/CO2 COMBO KTI

K-Number: K960468 · 1996-04-26

ApplicantNellcor Puritan Bennett, Inc.
Decision Date1996-04-26
Product CodeBTM
Advisory CommitteeAN
DecisionUnknown

Device Summary

DMR/CO2 COMBO KTI is the device name listed in this FDA 510(k) record. The listed applicant is Nellcor Puritan Bennett, Inc.. It received FDA 510(k) clearance on 1996-04-26 under 510(k) number K960468. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DMR/CO2 COMBO KTI?

DMR/CO2 COMBO KTI is a medical device that received FDA 510(k) clearance on 1996-04-26. The listed applicant is Nellcor Puritan Bennett, Inc.. The 510(k) number is K960468.

When did DMR/CO2 COMBO KTI receive FDA 510(k) clearance?

DMR/CO2 COMBO KTI received FDA 510(k) clearance on 1996-04-26, under 510(k) number K960468.

Who is the listed applicant for DMR/CO2 COMBO KTI?

The FDA 510(k) record lists Nellcor Puritan Bennett, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DMR/CO2 COMBO KTI?

The FDA product code for DMR/CO2 COMBO KTI is BTM.

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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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