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

Cresol Red Colorimetry, Carbon-Dioxide

21 CFR 862.1160 / Clinical Chemistry
FDA source (opens on fda.gov)

CIL is the FDA product code for Cresol Red Colorimetry, Carbon-Dioxide, a class II device type, regulated under 21 CFR 862.1160. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CIL
Device name
Cresol Red Colorimetry, Carbon-Dioxide
Regulation
21 CFR 862.1160
Device class
Class II
Review panel
Clinical Chemistry
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
4
Ingested recalls
0

Clearances, product code CIL

By decision year
4 clearances under product code CIL with a decision year between 1980 and 1992, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CIL by decision year
YearClearances
19801
19831
19891
19921

Applicants with the most clearances

Product code CIL
Applicants holding the most 510(k) clearances under product code CIL
ApplicantClearances
American Monitor Corp.2
Boehringer Mannheim Corp.1
Em Diagnostic Systems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code CIL.