ALGO 3I NEWBORN HEARING SCREENER
K-Number: K030823 · 2003-04-09
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Device Summary
Frequently Asked Questions
What is the ALGO 3I NEWBORN HEARING SCREENER?
ALGO 3I NEWBORN HEARING SCREENER is a medical device that received FDA 510(k) clearance on 2003-04-09. The listed applicant is Natus Medical, Inc.. The 510(k) number is K030823.
When did ALGO 3I NEWBORN HEARING SCREENER receive FDA 510(k) clearance?
ALGO 3I NEWBORN HEARING SCREENER received FDA 510(k) clearance on 2003-04-09, under 510(k) number K030823.
Who is the listed applicant for ALGO 3I NEWBORN HEARING SCREENER?
The FDA 510(k) record lists Natus Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALGO 3I NEWBORN HEARING SCREENER?
The FDA product code for ALGO 3I NEWBORN HEARING SCREENER is GWJ.
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, 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: GWJ)
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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