TYPE 9293 INTERFACE PULSEOX
K-Number: K896738 · 1990-08-14
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Device Summary
Frequently Asked Questions
What is the TYPE 9293 INTERFACE PULSEOX?
TYPE 9293 INTERFACE PULSEOX is a medical device that received FDA 510(k) clearance on 1990-08-14. The listed applicant is S & W Medico Teknik. The 510(k) number is K896738.
When did TYPE 9293 INTERFACE PULSEOX receive FDA 510(k) clearance?
TYPE 9293 INTERFACE PULSEOX received FDA 510(k) clearance on 1990-08-14, under 510(k) number K896738.
Who is the listed applicant for TYPE 9293 INTERFACE PULSEOX?
The FDA 510(k) record lists S & W Medico Teknik as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TYPE 9293 INTERFACE PULSEOX?
The FDA product code for TYPE 9293 INTERFACE PULSEOX 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 S & W Medico Teknik 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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