Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K831313Substantially Equivalent

Tissue-Tek V.i.p. 100/200

Miles Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent

K831313 is the FDA 510(k) clearance record for TISSUE-TEK V.I.P. 100/200, a class I device, cleared for Miles Laboratories, Inc. on under FDA product code IEO (Processor, Tissue, Automated). FDA records list 158 510(k) clearances for Miles Laboratories, Inc., from to . As of , FDA records show no recalls naming K831313.

Clearance record

Decision date
Received
(97 days to decision)
Product code
IEO Processor, Tissue, Automated
Regulation
21 CFR 864.3875
Device class
Class I
Review panel
Pathology
Applicant
Miles Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code IEO

Trailing 12 months

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

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