510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K802563Substantially Equivalent

Transette System/collection & Transp

Inolex Corp./Div of Biomedical, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802563 is the FDA 510(k) clearance record for TRANSETTE SYSTEM/COLLECTION & TRANSP, a class I device, cleared for Inolex Corp./Div of Biomedical on under FDA product code JTW (System, Transport, Aerobic). FDA records list 2 510(k) clearances for Inolex Corp./Div of Biomedical, from to . As of , FDA records show no recalls naming K802563.

Clearance record

Decision date
Received
(15 days to decision)
Product code
JTW System, Transport, Aerobic
Regulation
21 CFR 866.2900
Device class
Class I
Review panel
Microbiology
Applicant
Inolex Corp./Div of Biomedical 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JTW

Trailing 12 months

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

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