510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K852117Substantially Equivalent

Cyto-Tek Centrifuge

Miles Laboratories, Inc., Elkhart IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K852117 is the FDA 510(k) clearance record for CYTO-TEK CENTRIFUGE, a class I device, cleared for Miles Laboratories, Inc. on under FDA product code IFB (Cytocentrifuge). FDA records list 158 510(k) clearances for Miles Laboratories, Inc., from to . As of , FDA records show no recalls naming K852117.

Clearance record

Decision date
Received
(26 days to decision)
Product code
IFB Cytocentrifuge
Regulation
21 CFR 864.3300
Device class
Class I
Review panel
Pathology
Applicant
Miles Laboratories, Inc. 1127 Myrtle St., Elkhart IN
Third party review
No

Clearances, product code IFB

Trailing 12 months

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

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