FINGERTIP PULSE OXIMETER, MODEL CMS-50C
K-Number: K073454 · 2008-05-05
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Device Summary
Frequently Asked Questions
What is the FINGERTIP PULSE OXIMETER, MODEL CMS-50C?
FINGERTIP PULSE OXIMETER, MODEL CMS-50C is a medical device that received FDA 510(k) clearance on 2008-05-05. The listed applicant is Contec Medical System Co., Ltd.. The 510(k) number is K073454.
When did FINGERTIP PULSE OXIMETER, MODEL CMS-50C receive FDA 510(k) clearance?
FINGERTIP PULSE OXIMETER, MODEL CMS-50C received FDA 510(k) clearance on 2008-05-05, under 510(k) number K073454.
Who is the listed applicant for FINGERTIP PULSE OXIMETER, MODEL CMS-50C?
The FDA 510(k) record lists Contec Medical System Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FINGERTIP PULSE OXIMETER, MODEL CMS-50C?
The FDA product code for FINGERTIP PULSE OXIMETER, MODEL CMS-50C 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 Contec Medical System Co., Ltd. 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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