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FDA 510(k)

NPB-290 PULSE OXIMETER (NPB-290)

K-Number: K972837 · 1997-10-21

Decision Date1997-10-21
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NPB-290 PULSE OXIMETER (NPB-290) 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 1997-10-21 under 510(k) number K972837. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NPB-290 PULSE OXIMETER (NPB-290)?

NPB-290 PULSE OXIMETER (NPB-290) is a medical device that received FDA 510(k) clearance on 1997-10-21. The listed applicant is Nellcor Puritan Bennett, Inc.. The 510(k) number is K972837.

When did NPB-290 PULSE OXIMETER (NPB-290) receive FDA 510(k) clearance?

NPB-290 PULSE OXIMETER (NPB-290) received FDA 510(k) clearance on 1997-10-21, under 510(k) number K972837.

Who is the listed applicant for NPB-290 PULSE OXIMETER (NPB-290)?

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 NPB-290 PULSE OXIMETER (NPB-290)?

The FDA product code for NPB-290 PULSE OXIMETER (NPB-290) is DQA.

Related Clinical Trials

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.

Other records listing Nellcor Puritan Bennett, Inc. as applicant

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.

View all 42 devices →

Related Devices (Code: DQA)

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.

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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