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

Rhinoanemometer (Measurement Of Nasal Decongestion)

21 CFR 868.1800 / Anesthesiology
FDA source (opens on fda.gov)

BXQ is the FDA product code for Rhinoanemometer (Measurement Of Nasal Decongestion), a class II device type, regulated under 21 CFR 868.1800. As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
BXQ
Device name
Rhinoanemometer (Measurement Of Nasal Decongestion)
Regulation
21 CFR 868.1800
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
12
Ingested recalls
0

Clearances, product code BXQ

By decision year
12 clearances under product code BXQ with a decision year between 1984 and 2022, 1985 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code BXQ by decision year
YearClearances
19841
19852
19902
19931
19981
20001
20022
20171
20221

Applicants with the most clearances

Product code BXQ
Applicants holding the most 510(k) clearances under product code BXQ
ApplicantClearances
Rhino Metrics A/S2
And/Or Corp.1
Center Laboratories, Inc.1
E. Benson Hood Lab, Inc.1
G.M. Instruments Ltd.1
Hood Laboratories1
Intertronic, Inc.1
JEDMED Instrument Company1
Life-Tech Intl., Inc.1
Pacificmd Biotech, LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code