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FDA 510(k)

OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR

K-Number: K033973 · 2004-12-13

ApplicantNellcor Puritan Bennett, Inc.
Decision Date2004-12-13
Product CodeNLF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR 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 2004-12-13 under 510(k) number K033973. The device is classified under product code NLF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR?

OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR is a medical device that received FDA 510(k) clearance on 2004-12-13. The listed applicant is Nellcor Puritan Bennett, Inc.. The 510(k) number is K033973.

When did OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR receive FDA 510(k) clearance?

OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR received FDA 510(k) clearance on 2004-12-13, under 510(k) number K033973.

Who is the listed applicant for OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR?

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 OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR?

The FDA product code for OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR is NLF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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