SPO2 FINGER PROBES
K-Number: K973970 · 1998-10-06
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Device Summary
Frequently Asked Questions
What is the SPO2 FINGER PROBES?
SPO2 FINGER PROBES is a medical device that received FDA 510(k) clearance on 1998-10-06. The listed applicant is Medical Cables, Inc.. The 510(k) number is K973970.
When did SPO2 FINGER PROBES receive FDA 510(k) clearance?
SPO2 FINGER PROBES received FDA 510(k) clearance on 1998-10-06, under 510(k) number K973970.
Who is the listed applicant for SPO2 FINGER PROBES?
The FDA 510(k) record lists Medical Cables, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPO2 FINGER PROBES?
The FDA product code for SPO2 FINGER PROBES 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 Medical Cables, 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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