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

Bottle, Collection And Trap, Breathing System (Uncalibrated)

21 CFR 880.6740 / General Hospital
FDA source (opens on fda.gov)

CBC is the FDA product code for Bottle, Collection And Trap, Breathing System (Uncalibrated), a class II device type, regulated under 21 CFR 880.6740. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CBC
Device name
Bottle, Collection And Trap, Breathing System (Uncalibrated)
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code CBC

By decision year
3 clearances under product code CBC with a decision year between 1976 and 1993, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CBC by decision year
YearClearances
19761
19791
19931

Applicants with the most clearances

Product code CBC
Applicants holding the most 510(k) clearances under product code CBC
ApplicantClearances
Bird Products Corp.1
Inspiron Corp.1
Narco Air-Shields1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 16 companies shown, in name order