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

Flowmeter, Tube, Thorpe, Back-Pressure Compensated

21 CFR 868.2340 / Anesthesiology
FDA source (opens on fda.gov)

CAX is the FDA product code for Flowmeter, Tube, Thorpe, Back-Pressure Compensated, a class I device type, regulated under 21 CFR 868.2340. As of , FDA records hold 24 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
CAX
Device name
Flowmeter, Tube, Thorpe, Back-Pressure Compensated
Regulation
21 CFR 868.2340
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
24
Ingested recalls
1

Clearances, product code CAX

By decision year
24 clearances under product code CAX with a decision year between 1976 and 1993, 1979 the highest year at 5.
Show the numbers
510(k) clearances under FDA product code CAX by decision year
YearClearances
19762
19781
19795
19802
19813
19841
19854
19861
19872
19891
19911
19931

Applicants with the most clearances

Product code CAX
Applicants holding the most 510(k) clearances under product code CAX
ApplicantClearances
Timeter Instrument Corp.6
Precision Medical, Inc.3
Precision Metering, Inc.2
Airco, Inc.1
Bar-Dix, Inc.1
Chemetron Medical Products, Inc.1
Design & Manufacturing Consultants1
Harris Calorific1
Harris-Lake, Inc.1
Key Instruments1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 44 companies shown, in name order