510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
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K811437Substantially Equivalent

Modified Thoracentesis Catheter

Blair Medical Products, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811437 is the FDA 510(k) clearance record for MODIFIED THORACENTESIS CATHETER, a class II device, cleared for Blair Medical Products on under FDA product code KDQ (Bottle, Collection, Vacuum). FDA records list one 510(k) clearance for Blair Medical Products. As of , FDA records show no recalls naming K811437.

Clearance record

Decision date
Received
(83 days to decision)
Product code
KDQ Bottle, Collection, Vacuum
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
Blair Medical Products 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KDQ

Trailing 12 months

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

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