510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K832865Substantially Equivalent

Flex Bubble Tubing

Sheridan Catheter Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832865 is the FDA 510(k) clearance record for FLEX BUBBLE TUBING, a class II device, cleared for Sheridan Catheter Corp. on under FDA product code BYY (Tube, Aspirating, Flexible, Connecting). FDA records list 39 510(k) clearances for Sheridan Catheter Corp., from to . As of , FDA records show no recalls naming K832865.

Clearance record

Decision date
Received
(37 days to decision)
Product code
BYY Tube, Aspirating, Flexible, Connecting
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
Sheridan Catheter Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code BYY

Trailing 12 months

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

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