510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K853569Substantially Equivalent

Medipart Corrugated Polyethylene & E.v.a. Tubing

Medipart Jerry Alexander, Cary IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K853569 is the FDA 510(k) clearance record for MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING, a class I device, cleared for Medipart Jerry Alexander on under FDA product code BYX (Tubing, Pressure And Accessories). FDA records list 49 510(k) clearances for Medipart Jerry Alexander, from to . As of , FDA records show no recalls naming K853569.

Clearance record

Decision date
Received
(73 days to decision)
Product code
BYX Tubing, Pressure And Accessories
Regulation
21 CFR 868.5860
Device class
Class I
Review panel
Anesthesiology
Applicant
Medipart Jerry Alexander 607 Spring Beach Rd., Cary IL
Third party review
No

Clearances, product code BYX

Trailing 12 months

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

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