NON-INVASIVE INFRARED (NIR)
K-Number: K090386 · 2010-05-28
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Device Summary
Frequently Asked Questions
What is the NON-INVASIVE INFRARED (NIR)?
NON-INVASIVE INFRARED (NIR) is a medical device that received FDA 510(k) clearance on 2010-05-28. The listed applicant is Medisim, Ltd.. The 510(k) number is K090386.
When did NON-INVASIVE INFRARED (NIR) receive FDA 510(k) clearance?
NON-INVASIVE INFRARED (NIR) received FDA 510(k) clearance on 2010-05-28, under 510(k) number K090386.
Who is the listed applicant for NON-INVASIVE INFRARED (NIR)?
The FDA 510(k) record lists Medisim, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-INVASIVE INFRARED (NIR)?
The FDA product code for NON-INVASIVE INFRARED (NIR) is FLL.
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 Medisim, 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: FLL)
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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