FDA 510(k)

NELLCOR PURITAN BENNETT ACHIEVA VENTILATOR AND REPORT GENERATOR

K-Number: K990177 · 1999-11-18

Decision Date1999-11-18

Product CodeCBK

Advisory CommitteeAN

DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

NELLCOR PURITAN BENNETT ACHIEVA VENTILATOR AND REPORT GENERATOR 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 1999-11-18 under 510(k) number K990177. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the NELLCOR PURITAN BENNETT ACHIEVA VENTILATOR AND REPORT GENERATOR?

NELLCOR PURITAN BENNETT ACHIEVA VENTILATOR AND REPORT GENERATOR is a medical device that received FDA 510(k) clearance on 1999-11-18. The listed applicant is Nellcor Puritan Bennett, Inc.. The 510(k) number is K990177.

When did NELLCOR PURITAN BENNETT ACHIEVA VENTILATOR AND REPORT GENERATOR receive FDA 510(k) clearance?

NELLCOR PURITAN BENNETT ACHIEVA VENTILATOR AND REPORT GENERATOR received FDA 510(k) clearance on 1999-11-18, under 510(k) number K990177.

Who is the listed applicant for NELLCOR PURITAN BENNETT ACHIEVA VENTILATOR AND REPORT GENERATOR?

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 NELLCOR PURITAN BENNETT ACHIEVA VENTILATOR AND REPORT GENERATOR?

The FDA product code for NELLCOR PURITAN BENNETT ACHIEVA VENTILATOR AND REPORT GENERATOR is CBK.

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Other records listing Nellcor Puritan Bennett, Inc. as applicant

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Related Devices (Code: CBK)

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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.