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

Nebulizer, Medicinal, Non-Ventilatory (Atomizer)

21 CFR 868.5640 / Anesthesiology
FDA source (opens on fda.gov)

CCQ is the FDA product code for Nebulizer, Medicinal, Non-Ventilatory (Atomizer), a class I device type, regulated under 21 CFR 868.5640. As of , FDA records hold 62 510(k) clearances under this code, the most recent dated , and 9 recalls.

Classification record

Product code
CCQ
Device name
Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
Regulation
21 CFR 868.5640
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
62
Ingested recalls
9

Clearances, product code CCQ

By decision year
62 clearances under product code CCQ with a decision year between 1976 and 1997, 1984 the highest year at 12.
Show the numbers
510(k) clearances under FDA product code CCQ by decision year
YearClearances
19761
19782
19802
19813
19822
19832
198412
19859
19863
19878
19882
19894
19904
19912
19921
19963
19972

Applicants with the most clearances

Product code CCQ
Applicants holding the most 510(k) clearances under product code CCQ
ApplicantClearances
Armour Pharmaceutical Co.5
Monaghan Medical Corp.3
Vortran Medical Technology 1, Inc3
Devilbiss Health Care, Inc.2
Dey Laboratories, Inc.2
Dhd Medical Products Div. Diemolding Corp.2
Key Pharmaceuticals, Inc.2
Medipart Jerry Alexander2
Salter Labs2
The Devilbiss Co.2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 139 companies shown, in name order