FDA PMA FDA Class 2 Approved 🇺🇸 United States

Sharps Needle Destruction Device

PMA: P980015 · Supplement: S001 · Decision Dec 14, 1998
Classifications
1
FEI Numbers
0
Registration Numbers
0

Basic Information

Device Name
Sharps Needle Destruction Device
Trade Name
SHARP NEEDLE DESTRUCTION UNIT
PMA Number
P980015
Supplement Number
S001
Device Class
FDA Class 2
Product Code
MTV
Generic Name
Sharps needle destruction device
Regulation Number
880.6210
Medical Specialty
General Hospital
Advisory Committee
General Hospital
Decision
Approved
Decision Code
APPR
Decision Date
December 14, 1998
Date Received
December 8, 1998
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for the modifications of device and to the labeling. The modifications to the device were noted to include the addition of a charger base and modifications to the device housing, electrode assembly and filter.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MTV Sharps Needle Destruction Device