NXSTAGE PUREFLOW SL— 510(k) K140571

Substantially Equivalent

Nxstage Medical, Inc.

FDA 510(k) clearance K140571 for NXSTAGE PUREFLOW SL, Substantially Equivalent on 2014-05-15. 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 ↗

Recent devices under product code FKR

view all

More clearances from Nxstage Medical, Inc.

view all

Recalls naming K140571

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 K140571.

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