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

Pump, Nebulizer, Electrically Powered

21 CFR 874.5220 / Ear, Nose, Throat
FDA source (opens on fda.gov)

JPW is the FDA product code for Pump, Nebulizer, Electrically Powered, a class I device type, regulated under 21 CFR 874.5220. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
JPW
Device name
Pump, Nebulizer, Electrically Powered
Regulation
21 CFR 874.5220
Device class
Class I
Review panel
Ear, Nose, Throat
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 JPW

By decision year
1 clearance under product code JPW with a decision year between 1983 and 1983, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JPW by decision year
YearClearances
19831

Applicants with the most clearances

Product code JPW
Applicants holding the most 510(k) clearances under product code JPW
ApplicantClearances
Buckman Co., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 33 companies shown, in name order