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

Exerciser, Finger, Powered

21 CFR 890.5410 / Physical Medicine
FDA source (opens on fda.gov)

JFA is the FDA product code for Exerciser, Finger, Powered, a class I device type, regulated under 21 CFR 890.5410. As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JFA
Device name
Exerciser, Finger, Powered
Regulation
21 CFR 890.5410
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
12
Ingested recalls
0

Clearances, product code JFA

By decision year
12 clearances under product code JFA with a decision year between 1979 and 1995, 1988 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JFA by decision year
YearClearances
19791
19831
19841
19861
19882
19902
19921
19942
19951

Applicants with the most clearances

Product code JFA
Applicants holding the most 510(k) clearances under product code JFA
ApplicantClearances
Toronto Medical Corp.3
Buckman Co., Inc.2
Jace Systems, Inc.2
Bardon Ent., Inc.1
Burke Neutech, Inc.1
Danninger Medical Technology, Inc.1
Maddak, Inc.1
Sutter Biomedical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 20 companies shown, in name order