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

Dropper, Ether

21 CFR 868.5420 / Anesthesiology
FDA source (opens on fda.gov)

BTP is the FDA product code for Dropper, Ether, a class I device type, regulated under 21 CFR 868.5420. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
BTP
Device name
Dropper, Ether
Regulation
21 CFR 868.5420
Device class
Class I
Review panel
Anesthesiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code BTP

By decision year
1 clearance under product code BTP with a decision year between 2010 and 2010, 2010 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code BTP by decision year
YearClearances
20101

Applicants with the most clearances

Product code BTP
Applicants holding the most 510(k) clearances under product code BTP
ApplicantClearances
Hospitech Respiration1

Companies listing this code with FDA

Companies whose registered establishments list this code