510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K110409Substantially Equivalent

Aspira Pleural Drainage System

C.R. Bard Inc, Salt Lake Ciy, UT / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K110409 is the FDA 510(k) clearance record for ASPIRA PLEURAL DRAINAGE SYSTEM, a class II device, cleared for C.R. Bard, Inc. on under FDA product code DWM (Apparatus, Suction, Patient Care). FDA records list 646 510(k) clearances for C.R. Bard, Inc., from to . As of , FDA records show one recall naming K110409.

Clearance record

Decision date
Received
(86 days to decision)
Product code
DWM Apparatus, Suction, Patient Care
Regulation
21 CFR 870.5050
Device class
Class II
Review panel
Cardiovascular
Applicant
C.R. Bard, Inc. 605 N. 5600 W., Salt Lake Ciy, UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DWM

Trailing 12 months

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

FDA records show no clearances under product code DWM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DWM, 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