NXSTAGE DIALYSATE PREPARATION MODULE
K-Number: K060296 · 2006-03-31
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Device Summary
Frequently Asked Questions
What is the NXSTAGE DIALYSATE PREPARATION MODULE?
NXSTAGE DIALYSATE PREPARATION MODULE is a medical device that received FDA 510(k) clearance on 2006-03-31. The listed applicant is Nxstage Medical, Inc.. The 510(k) number is K060296.
When did NXSTAGE DIALYSATE PREPARATION MODULE receive FDA 510(k) clearance?
NXSTAGE DIALYSATE PREPARATION MODULE received FDA 510(k) clearance on 2006-03-31, under 510(k) number K060296.
Who is the listed applicant for NXSTAGE DIALYSATE PREPARATION MODULE?
The FDA 510(k) record lists Nxstage Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NXSTAGE DIALYSATE PREPARATION MODULE?
The FDA product code for NXSTAGE DIALYSATE PREPARATION MODULE is FKR.
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 Nxstage 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: FKR)
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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