PB VIDEO DISPLAY TO PB251 PULSE OXIMETER UPGRADE
K-Number: K871826 · 1987-06-29
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Device Summary
Frequently Asked Questions
What is the PB VIDEO DISPLAY TO PB251 PULSE OXIMETER UPGRADE?
PB VIDEO DISPLAY TO PB251 PULSE OXIMETER UPGRADE is a medical device that received FDA 510(k) clearance on 1987-06-29. The listed applicant is Datex Division Instrumentarium Corp.. The 510(k) number is K871826.
When did PB VIDEO DISPLAY TO PB251 PULSE OXIMETER UPGRADE receive FDA 510(k) clearance?
PB VIDEO DISPLAY TO PB251 PULSE OXIMETER UPGRADE received FDA 510(k) clearance on 1987-06-29, under 510(k) number K871826.
Who is the listed applicant for PB VIDEO DISPLAY TO PB251 PULSE OXIMETER UPGRADE?
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 PB VIDEO DISPLAY TO PB251 PULSE OXIMETER UPGRADE?
The FDA product code for PB VIDEO DISPLAY TO PB251 PULSE OXIMETER UPGRADE 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 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: 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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