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

Absorbent, Carbon-Dioxide

21 CFR 868.5300 / Anesthesiology
FDA source (opens on fda.gov)

CBL is the FDA product code for Absorbent, Carbon-Dioxide, a class I device type, regulated under 21 CFR 868.5300. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and 7 recalls.

Classification record

Product code
CBL
Device name
Absorbent, Carbon-Dioxide
Regulation
21 CFR 868.5300
Device class
Class I
Review panel
Anesthesiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
5
Ingested recalls
7

Clearances, product code CBL

By decision year
5 clearances under product code CBL with a decision year between 1981 and 1992, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CBL by decision year
YearClearances
19811
19851
19861
19901
19921

Applicants with the most clearances

Product code CBL
Applicants holding the most 510(k) clearances under product code CBL
ApplicantClearances
Allied Medical LLC1
Dentsply Intl.1
Gibeck, Inc.1
Medipart Jerry Alexander1
Molecular Products Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 24 companies shown, in name order