REUSABLE FINGER CLIP SPO2 SENSORS
K-Number: K042704 · 2004-11-26
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Device Summary
Frequently Asked Questions
What is the REUSABLE FINGER CLIP SPO2 SENSORS?
REUSABLE FINGER CLIP SPO2 SENSORS is a medical device that received FDA 510(k) clearance on 2004-11-26. The listed applicant is Elekon Industries U.S.A., Inc.. The 510(k) number is K042704.
When did REUSABLE FINGER CLIP SPO2 SENSORS receive FDA 510(k) clearance?
REUSABLE FINGER CLIP SPO2 SENSORS received FDA 510(k) clearance on 2004-11-26, under 510(k) number K042704.
Who is the listed applicant for REUSABLE FINGER CLIP SPO2 SENSORS?
The FDA 510(k) record lists Elekon Industries U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REUSABLE FINGER CLIP SPO2 SENSORS?
The FDA product code for REUSABLE FINGER CLIP SPO2 SENSORS 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 Elekon Industries U.S.A., 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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