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

Solution, Zenker'S

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

IFH is the FDA product code for Solution, Zenker'S, a class I device type, regulated under 21 CFR 864.4010. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IFH
Device name
Solution, Zenker'S
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
2
Ingested recalls
0

Clearances, product code IFH

By decision year
2 clearances under product code IFH with a decision year between 1982 and 1984, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IFH by decision year
YearClearances
19821
19841

Applicants with the most clearances

Product code IFH
Applicants holding the most 510(k) clearances under product code IFH
ApplicantClearances
E K Ind., Inc.1
Volu Sol Medical Industries1

Companies listing this code with FDA

Companies whose registered establishments list this code