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

Attachment, Intermittent Mandatory Ventilation (Imv)

21 CFR 868.5955 / Anesthesiology
FDA source (opens on fda.gov)

CBO is the FDA product code for Attachment, Intermittent Mandatory Ventilation (Imv), a class II device type, regulated under 21 CFR 868.5955. As of , FDA records hold 15 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CBO
Device name
Attachment, Intermittent Mandatory Ventilation (Imv)
Regulation
21 CFR 868.5955
Device class
Class II
Review panel
Anesthesiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
Yes
GMP exempt
No
Third party review eligible
No
Ingested clearances
15
Ingested recalls
0

Clearances, product code CBO

By decision year
15 clearances under product code CBO with a decision year between 1976 and 1981, 1979 the highest year at 8.
Show the numbers
510(k) clearances under FDA product code CBO by decision year
YearClearances
19765
19798
19812

Applicants with the most clearances

Product code CBO
Applicants holding the most 510(k) clearances under product code CBO
ApplicantClearances
Mem Medical, Inc.7
Airlife, Inc.1
B & F Medical Products, Inc.1
BD Becton Dickinson Vacutainer Systems Preanalytic1
Chemetron Medical Products, Inc.1
Foregger1
Inspiron Corp.1
Manner Medical Products1
The Lynn Terrell Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code