OSCILLOMATE NIBP / SP02 EMS MONITOR
K-Number: K980879 · 1998-07-16
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Device Summary
Frequently Asked Questions
What is the OSCILLOMATE NIBP / SP02 EMS MONITOR?
OSCILLOMATE NIBP / SP02 EMS MONITOR is a medical device that received FDA 510(k) clearance on 1998-07-16. The listed applicant is Cas Medical Systems, Inc.. The 510(k) number is K980879.
When did OSCILLOMATE NIBP / SP02 EMS MONITOR receive FDA 510(k) clearance?
OSCILLOMATE NIBP / SP02 EMS MONITOR received FDA 510(k) clearance on 1998-07-16, under 510(k) number K980879.
Who is the listed applicant for OSCILLOMATE NIBP / SP02 EMS MONITOR?
The FDA 510(k) record lists Cas Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSCILLOMATE NIBP / SP02 EMS MONITOR?
The FDA product code for OSCILLOMATE NIBP / SP02 EMS MONITOR 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 Cas Medical Systems, 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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