510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K961155Substantially Equivalent

Solo Picc/midline Catheter Kit Models 71924, 71908

Douglas Medical Products, Inc, Libertyville IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K961155 is the FDA 510(k) clearance record for SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908, a class II device, cleared for Douglas Medical Products Corp. on under FDA product code LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days). FDA records list 20 510(k) clearances for Douglas Medical Products Corp., from to . As of , FDA records show no recalls naming K961155.

Clearance record

Decision date
Received
(88 days to decision)
Product code
LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Regulation
21 CFR 880.5970
Device class
Class II
Review panel
General Hospital
Applicant
Douglas Medical Products Corp. 1840 Industrial Dr., Suite 200, Libertyville IL
510(k) summary
Summary
Third party review
No

Clearances, product code LJS

Trailing 12 months
3 clearances under product code LJS in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LJS, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260