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FDA 510(k)

SUZANNE

K-Number: K990565 · 1999-08-18

ApplicantNellcor Puritan Bennett, Inc.
Decision Date1999-08-18
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SUZANNE 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 1999-08-18 under 510(k) number K990565. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUZANNE?

SUZANNE is a medical device that received FDA 510(k) clearance on 1999-08-18. The listed applicant is Nellcor Puritan Bennett, Inc.. The 510(k) number is K990565.

When did SUZANNE receive FDA 510(k) clearance?

SUZANNE received FDA 510(k) clearance on 1999-08-18, under 510(k) number K990565.

Who is the listed applicant for SUZANNE?

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 SUZANNE?

The FDA product code for SUZANNE is MNR.

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Other records listing Nellcor Puritan Bennett, 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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