SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES
K-Number: K093853 · 2010-06-04
Advertisement
Device Summary
Frequently Asked Questions
What is the SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES?
SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES is a medical device that received FDA 510(k) clearance on 2010-06-04. The listed applicant is Nonin Medical, Inc.. The 510(k) number is K093853.
When did SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES receive FDA 510(k) clearance?
SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES received FDA 510(k) clearance on 2010-06-04, under 510(k) number K093853.
Who is the listed applicant for SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES?
The FDA 510(k) record lists Nonin Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES?
The FDA product code for SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES 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 Nonin Medical, 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.
Advertisement