NEOBLUE BLANKET LED PHOTOTHERAPY SYSTEM
K-Number: K103589 · 2011-05-13
Advertisement
Device Summary
Frequently Asked Questions
What is the NEOBLUE BLANKET LED PHOTOTHERAPY SYSTEM?
NEOBLUE BLANKET LED PHOTOTHERAPY SYSTEM is a medical device that received FDA 510(k) clearance on 2011-05-13. The listed applicant is Natus Medical Incorporated. The 510(k) number is K103589.
When did NEOBLUE BLANKET LED PHOTOTHERAPY SYSTEM receive FDA 510(k) clearance?
NEOBLUE BLANKET LED PHOTOTHERAPY SYSTEM received FDA 510(k) clearance on 2011-05-13, under 510(k) number K103589.
Who is the listed applicant for NEOBLUE BLANKET LED PHOTOTHERAPY SYSTEM?
The FDA 510(k) record lists Natus Medical Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEOBLUE BLANKET LED PHOTOTHERAPY SYSTEM?
The FDA product code for NEOBLUE BLANKET LED PHOTOTHERAPY SYSTEM is LBI.
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 Natus Medical Incorporated 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: LBI)
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.
Advertisement