AMERIWATER PURIFICATION SYSTEM FOR HEMODIALYSIS
K-Number: K991519 · 2000-04-14
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Device Summary
Frequently Asked Questions
What is the AMERIWATER PURIFICATION SYSTEM FOR HEMODIALYSIS?
AMERIWATER PURIFICATION SYSTEM FOR HEMODIALYSIS is a medical device that received FDA 510(k) clearance on 2000-04-14. The listed applicant is Ameriwater. The 510(k) number is K991519.
When did AMERIWATER PURIFICATION SYSTEM FOR HEMODIALYSIS receive FDA 510(k) clearance?
AMERIWATER PURIFICATION SYSTEM FOR HEMODIALYSIS received FDA 510(k) clearance on 2000-04-14, under 510(k) number K991519.
Who is the listed applicant for AMERIWATER PURIFICATION SYSTEM FOR HEMODIALYSIS?
The FDA 510(k) record lists Ameriwater as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMERIWATER PURIFICATION SYSTEM FOR HEMODIALYSIS?
The FDA product code for AMERIWATER PURIFICATION SYSTEM FOR HEMODIALYSIS is FIP.
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 Ameriwater 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: FIP)
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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