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

Cytocentrifuge

21 CFR 864.3300 / Pathology
FDA source (opens on fda.gov)

IFB is the FDA product code for Cytocentrifuge, a class I device type, regulated under 21 CFR 864.3300. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
IFB
Device name
Cytocentrifuge
Regulation
21 CFR 864.3300
Device class
Class I
Review panel
Pathology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
2

Clearances, product code IFB

By decision year
3 clearances under product code IFB with a decision year between 1979 and 1985, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IFB by decision year
YearClearances
19791
19811
19851

Applicants with the most clearances

Product code IFB
Applicants holding the most 510(k) clearances under product code IFB
ApplicantClearances
Cytochem, Inc.1
Miles Laboratories, Inc.1
Robert C. Leif, Ph.D.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 16 companies shown, in name order