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

Carbol Fuchsin

21 CFR 864.1850 / Hematology
FDA source (opens on fda.gov)

ICL is the FDA product code for Carbol Fuchsin, a class I device type, regulated under 21 CFR 864.1850. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
ICL
Device name
Carbol Fuchsin
Regulation
21 CFR 864.1850
Device class
Class I
Review panel
Hematology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
4
Ingested recalls
0

Clearances, product code ICL

By decision year
4 clearances under product code ICL with a decision year between 1977 and 1989, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code ICL by decision year
YearClearances
19771
19791
19841
19891

Applicants with the most clearances

Product code ICL
Applicants holding the most 510(k) clearances under product code ICL
ApplicantClearances
Alpha-Tec Systems, Inc.1
E K Ind., Inc.1
Harleco1
Laboratory Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 24 companies shown, in name order