510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K792032Substantially Equivalent

Leif Centrifugal Cytology Bucket

Robert C. Leif, Ph.D., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K792032 is the FDA 510(k) clearance record for LEIF CENTRIFUGAL CYTOLOGY BUCKET, a class I device, cleared for Robert C. Leif, Ph.D. on under FDA product code IFB (Cytocentrifuge). FDA records list one 510(k) clearance for Robert C. Leif, Ph.D. As of , FDA records show no recalls naming K792032.

Clearance record

Decision date
Received
(51 days to decision)
Product code
IFB Cytocentrifuge
Regulation
21 CFR 864.3300
Device class
Class I
Review panel
Pathology
Applicant
Robert C. Leif, Ph.D. 803 N. Front St. Suite 3, Mchenry IL
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