NERIA SOFT 90 INFUSION SET
K-Number: K132142 · 2013-10-08
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Device Summary
Frequently Asked Questions
What is the NERIA SOFT 90 INFUSION SET?
NERIA SOFT 90 INFUSION SET is a medical device that received FDA 510(k) clearance on 2013-10-08. The listed applicant is Unomedical A/S. The 510(k) number is K132142.
When did NERIA SOFT 90 INFUSION SET receive FDA 510(k) clearance?
NERIA SOFT 90 INFUSION SET received FDA 510(k) clearance on 2013-10-08, under 510(k) number K132142.
Who is the listed applicant for NERIA SOFT 90 INFUSION SET?
The FDA 510(k) record lists Unomedical A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NERIA SOFT 90 INFUSION SET?
The FDA product code for NERIA SOFT 90 INFUSION SET is FPA.
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 Unomedical A/S 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: FPA)
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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