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

Transducer, Gas Flow

21 CFR 868.2885 / Anesthesiology
FDA source (opens on fda.gov)

BXP is the FDA product code for Transducer, Gas Flow, a class I device type, regulated under 21 CFR 868.2885. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
BXP
Device name
Transducer, Gas Flow
Regulation
21 CFR 868.2885
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
7
Ingested recalls
0

Clearances, product code BXP

By decision year
7 clearances under product code BXP with a decision year between 1976 and 1994, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code BXP by decision year
YearClearances
19761
19771
19781
19801
19841
19921
19941

Applicants with the most clearances

Product code BXP
Applicants holding the most 510(k) clearances under product code BXP
ApplicantClearances
Chambers & Sadler Mfg.1
Kells Medical, Inc.1
Medical Fittings, Inc.1
The John Bunn Co.1
Revvity Health Sciences, Inc.1
Timeter Instrument Corp.1
Unipower Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 25 companies shown, in name order