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

Solution, Formalin-Alcohol-Acetic Acid

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

IGF is the FDA product code for Solution, Formalin-Alcohol-Acetic Acid, 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
IGF
Device name
Solution, Formalin-Alcohol-Acetic Acid
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 IGF

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

Applicants with the most clearances

Product code IGF
Applicants holding the most 510(k) clearances under product code IGF
ApplicantClearances
E K Ind., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 13 companies shown, in name order