OSCAR(TM) PB255 OXIMETER CAPNOMETER
K-Number: K872760 · 1987-09-14
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Device Summary
Frequently Asked Questions
What is the OSCAR(TM) PB255 OXIMETER CAPNOMETER?
OSCAR(TM) PB255 OXIMETER CAPNOMETER is a medical device that received FDA 510(k) clearance on 1987-09-14. The listed applicant is Datex Division Instrumentarium Corp.. The 510(k) number is K872760.
When did OSCAR(TM) PB255 OXIMETER CAPNOMETER receive FDA 510(k) clearance?
OSCAR(TM) PB255 OXIMETER CAPNOMETER received FDA 510(k) clearance on 1987-09-14, under 510(k) number K872760.
Who is the listed applicant for OSCAR(TM) PB255 OXIMETER CAPNOMETER?
The FDA 510(k) record lists Datex Division Instrumentarium Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSCAR(TM) PB255 OXIMETER CAPNOMETER?
The FDA product code for OSCAR(TM) PB255 OXIMETER CAPNOMETER is CCK.
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 Datex Division Instrumentarium Corp. 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: CCK)
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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