JOK — Scissors, Medical, Disposable Class I

FDA Device Classification

FDA product code JOK covers "Scissors, Medical, Disposable", a Class I medical device regulated under 21 CFR 880.6820. Submissions are reviewed by the General Hospital panel. At least 7 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
JOK
Device Class
Class I
Regulation Number
880.6820
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K855131dynarexSUTURE REMOVAL KITJanuary 13, 1986
K843075greene internationalUTILITY SCISSORS DISPOSABLE ITEMSSeptember 5, 1984
K812555medcare productsDISPOSABLE SUTURE REMOVAL SCISSORSNovember 16, 1981
K770595abco dealersSUTURE REMOVAL SETMay 23, 1977
K770481acme unitedSHEAR, PLASTIC HANDLE UTILITY S-475-7April 29, 1977
K770163conceptSUTURE CUTTERMarch 30, 1977
K761192superior plastic productsDRESSING CHANGE KITFebruary 28, 1977