510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K140571Substantially Equivalent

Nxstage Pureflow Sl

NxStage Medical Inc, Lawrence MA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K140571 is the FDA 510(k) clearance record for NXSTAGE PUREFLOW SL, a class II device, cleared for Nxstage Medical, Inc. on under FDA product code FKR (Subsystem, Proportioning). FDA records list 51 510(k) clearances for Nxstage Medical, Inc., from to . As of , FDA records show 9 recalls naming K140571.

Clearance record

Decision date
Received
(70 days to decision)
Product code
FKR Subsystem, Proportioning
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Nxstage Medical, Inc. 350 Merrimack St., Lawrence MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FKR

Trailing 12 months

FDA records hold no clearances under product code FKR in the trailing twelve months.

FDA records show no clearances under product code FKR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FKR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260