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

Locator, Acupuncture Point

21 CFR 880.5580 / General Hospital
FDA source (opens on fda.gov)

BWJ is the FDA product code for Locator, Acupuncture Point, a class II device type, regulated under 21 CFR 880.5580. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
BWJ
Device name
Locator, Acupuncture Point
Regulation
21 CFR 880.5580
Device class
Class II
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code BWJ

By decision year
3 clearances under product code BWJ with a decision year between 1978 and 1980, 1980 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code BWJ by decision year
YearClearances
19781
19802

Applicants with the most clearances

Product code BWJ
Applicants holding the most 510(k) clearances under product code BWJ
ApplicantClearances
Staodynamics, Inc.2
Ercona Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code