Home / Device Classification / KYQ

KYQ — Kit, Chemical Snake-Bite Class III

FDA Device Classification

FDA product code KYQ covers "Kit, Chemical Snake-Bite", a Class III medical device regulated under 21 CFR 880.5760. Submissions are reviewed by the General Hospital panel.

Classification Details

Product Code: KYQ
Device Class: Class III
Regulation Number: 880.5760
Submission Type
Review Panel: HO
Medical Specialty: General Hospital
Implant: No

Definition

Call for PMAs to be filed by 12/26/96 per 61 FR 50708 on 9/27/96