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

Acridine Orange

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

IDC is the FDA product code for Acridine Orange, 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
IDC
Device name
Acridine Orange
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 IDC

By decision year
4 clearances under product code IDC with a decision year between 1981 and 1985, 1981 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code IDC by decision year
YearClearances
19813
19851

Applicants with the most clearances

Product code IDC
Applicants holding the most 510(k) clearances under product code IDC
ApplicantClearances
Advanced Medical Technology, Inc.1
BD Becton Dickinson Vacutainer Systems Preanalytic1
Carr-Scarborough Microbiologicals, Inc.1
Remel Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code