NXSTAGE PUREFLOW SL— 510(k) K111174

Substantially Equivalent

Nxstage Medical, Inc.

FDA 510(k) clearance K111174 for NXSTAGE PUREFLOW SL, Substantially Equivalent on 2011-09-19. Applicant: Nxstage Medical, Inc.. Device class: 2.

Clearance details

Applicant
Nxstage Medical, Inc.
Product code
Code FKR
Device class
Class 2
Regulation
21 CFR 876.5820
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Lawrence, MA, US
Download summary PDFView on FDA.gov ↗

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Recalls naming K111174

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K111174.

Data sourced from openFDA. This site is unofficial and independent of the FDA.