NPB-190 PULSE OXIMETER (NPB-190)
K-Number: K971946 · 1997-08-25
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Device Summary
Frequently Asked Questions
What is the NPB-190 PULSE OXIMETER (NPB-190)?
NPB-190 PULSE OXIMETER (NPB-190) is a medical device that received FDA 510(k) clearance on 1997-08-25. The listed applicant is Nellcor Puritan Bennett, Inc.. The 510(k) number is K971946.
When did NPB-190 PULSE OXIMETER (NPB-190) receive FDA 510(k) clearance?
NPB-190 PULSE OXIMETER (NPB-190) received FDA 510(k) clearance on 1997-08-25, under 510(k) number K971946.
Who is the listed applicant for NPB-190 PULSE OXIMETER (NPB-190)?
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-190 PULSE OXIMETER (NPB-190)?
The FDA product code for NPB-190 PULSE OXIMETER (NPB-190) 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.
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
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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