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

Scissors, Medical, Disposable

21 CFR 880.6820 / General Hospital
FDA source (opens on fda.gov)

JOK is the FDA product code for Scissors, Medical, Disposable, a class I device type, regulated under 21 CFR 880.6820. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and 3 recalls.

Classification record

Product code
JOK
Device name
Scissors, Medical, Disposable
Regulation
21 CFR 880.6820
Device class
Class I
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
7
Ingested recalls
3

Clearances, product code JOK

By decision year
7 clearances under product code JOK with a decision year between 1977 and 1986, 1977 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code JOK by decision year
YearClearances
19774
19811
19841
19861

Applicants with the most clearances

Product code JOK
Applicants holding the most 510(k) clearances under product code JOK
ApplicantClearances
Abco Dealers, Inc.1
Acme United Corp.1
Concept, Inc.1
Dynarex Corp.1
Greene International Corp.1
Medcare Products1
Superior Plastic Products Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 163 companies shown, in name order