PSN HEMODIALYZER, MODELS PSN 170, PSN 210
K-Number: K001422 · 2000-06-02
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Device Summary
Frequently Asked Questions
What is the PSN HEMODIALYZER, MODELS PSN 170, PSN 210?
PSN HEMODIALYZER, MODELS PSN 170, PSN 210 is a medical device that received FDA 510(k) clearance on 2000-06-02. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K001422.
When did PSN HEMODIALYZER, MODELS PSN 170, PSN 210 receive FDA 510(k) clearance?
PSN HEMODIALYZER, MODELS PSN 170, PSN 210 received FDA 510(k) clearance on 2000-06-02, under 510(k) number K001422.
Who is the listed applicant for PSN HEMODIALYZER, MODELS PSN 170, PSN 210?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PSN HEMODIALYZER, MODELS PSN 170, PSN 210?
The FDA product code for PSN HEMODIALYZER, MODELS PSN 170, PSN 210 is KDI.
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 Baxter Healthcare Corp 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: KDI)
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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