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

Plethysmograph, Pressure

21 CFR 868.1750 / Anesthesiology
FDA source (opens on fda.gov)

CCM is the FDA product code for Plethysmograph, Pressure, a class II device type, regulated under 21 CFR 868.1750. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CCM
Device name
Plethysmograph, Pressure
Regulation
21 CFR 868.1750
Device class
Class II
Review panel
Anesthesiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
11
Ingested recalls
0

Clearances, product code CCM

By decision year
11 clearances under product code CCM with a decision year between 1978 and 2009, 1985 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code CCM by decision year
YearClearances
19781
19791
19854
19861
19891
19951
20031
20091

Applicants with the most clearances

Product code CCM
Applicants holding the most 510(k) clearances under product code CCM
ApplicantClearances
Erich Jaeger, Inc.4
Medical Graphics Corp.2
Hans Rudolph, Inc.1
Honeywell, Inc.1
Quinton, Inc.1
Viasys Healthcare GmbH1
Warren E. Collins, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code