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

Bottle, Collection, Breathing System (Calibrated)

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

CBD is the FDA product code for Bottle, Collection, Breathing System (Calibrated), 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
CBD
Device name
Bottle, Collection, Breathing System (Calibrated)
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 CBD

By decision year
3 clearances under product code CBD with a decision year between 1977 and 1978, 1977 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code CBD by decision year
YearClearances
19772
19781

Applicants with the most clearances

Product code CBD
Applicants holding the most 510(k) clearances under product code CBD
ApplicantClearances
Diemolding Corp.1
Lkb Instruments, Inc.1
Mcgaw Respiratory Therapy1

Companies listing this code with FDA

Companies whose registered establishments list this code