510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
IFIClass I

Sprays, Synthetic, Smear

21 CFR 864.4010 / Pathology
FDA source (opens on fda.gov)

IFI is the FDA product code for Sprays, Synthetic, Smear, a class I device type, regulated under 21 CFR 864.4010. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
IFI
Device name
Sprays, Synthetic, Smear
Regulation
21 CFR 864.4010
Device class
Class I
Review panel
Pathology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code IFI

By decision year
1 clearance under product code IFI with a decision year between 1980 and 1980, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IFI by decision year
YearClearances
19801

Applicants with the most clearances

Product code IFI
Applicants holding the most 510(k) clearances under product code IFI
ApplicantClearances
Laboratory Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code