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

Calibrator, Volume, Gas

21 CFR 868.1870 / Anesthesiology
FDA source (opens on fda.gov)

BXW is the FDA product code for Calibrator, Volume, Gas, a class I device type, regulated under 21 CFR 868.1870. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
BXW
Device name
Calibrator, Volume, Gas
Regulation
21 CFR 868.1870
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
6
Ingested recalls
0

Clearances, product code BXW

By decision year
6 clearances under product code BXW with a decision year between 1976 and 1985, 1981 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code BXW by decision year
YearClearances
19761
19812
19832
19851

Applicants with the most clearances

Product code BXW
Applicants holding the most 510(k) clearances under product code BXW
ApplicantClearances
Instrumentation Industries, Incorporated1
Mcgaw Laboratories1
Medical Graphics Corp.1
Ohio Medical Products1
Revvity Health Sciences, Inc.1
Timeter Instrument Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 15 companies shown, in name order