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

Airway, Nasopharyngeal

21 CFR 868.5100 / Anesthesiology
FDA source (opens on fda.gov)

BTQ is the FDA product code for Airway, Nasopharyngeal, a class I device type, regulated under 21 CFR 868.5100. As of , FDA records hold 19 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
BTQ
Device name
Airway, Nasopharyngeal
Regulation
21 CFR 868.5100
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
19
Ingested recalls
2

Clearances, product code BTQ

By decision year
19 clearances under product code BTQ with a decision year between 1976 and 1995, 1983 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code BTQ by decision year
YearClearances
19761
19791
19811
19833
19842
19852
19872
19881
19902
19912
19921
19951

Applicants with the most clearances

Product code BTQ
Applicants holding the most 510(k) clearances under product code BTQ
ApplicantClearances
Vesta, Inc.3
Polamedco, Inc.2
AD-Tech Medical Instrument Corp.1
Chatham Industries1
Coast Medical Corp.1
Dryden Corp.1
Eastmed Enterprises, Inc.1
Exmoor Plastics Limited1
Fls Medical Products, Inc.1
Harding Industries, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 119 companies shown, in name order