Product Code: JOK FDA class 1 21 CFR 880.6820

Scissors, Medical, Disposable

General Hospital

The Scissors, Medical, Disposable are single-use surgical scissors intended for general medical use in cutting tissue, sutures, bandages, or other materials during clinical procedures, after which they are discarded to prevent cross-contamination. This device is FDA Class 1, the lowest risk category, subject only to general controls such as proper labeling and manufacturing standards, with no premarket notification required. It carries product code JOK and is regulated under 21 CFR 880.6820, within the General Hospital medical specialty.

510(k)s
7
FEI Numbers
158
Registration Numbers
158
Unique Applicants
7
Years Active
9

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Basic Information

Product Code
JOK
Device Class
FDA class 1
Regulation Number
880.6820
Medical Specialty
General Hospital
Review Panel
HO
Submission Type
4

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

510(k) Clearance History

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Related 510(k) Clearances

This FDA classification is associated with 7 510(k) clearances via K numbers.

K Number Device Name
K855131 SUTURE REMOVAL KIT
K843075 UTILITY SCISSORS DISPOSABLE ITEMS
K812555 DISPOSABLE SUTURE REMOVAL SCISSORS
K770595 SUTURE REMOVAL SET
K770481 SHEAR, PLASTIC HANDLE UTILITY S-475-7
K770163 SUTURE CUTTER
K761192 DRESSING CHANGE KIT

FEI Numbers

This FDA classification entry is associated with 158 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 158 registration numbers. Click on an entry to view related FDA registrations.