FDA PMA FDA Class 2 Approved 🇺🇸 United States

Sharps Needle Destruction Device

PMA: P980015 · Supplement: S003 · Decision Sep 17, 1999
Classifications
1
FEI Numbers
0
Registration Numbers
0

Basic Information

Device Name
Sharps Needle Destruction Device
Trade Name
SHARP(X)TM NEEDLE DESTRUCTION UNIT
PMA Number
P980015
Supplement Number
S003
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
September 17, 1999
Date Received
September 14, 1999
Supplement Type
Real-Time Process
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for a modification of a contraindication statement in the labeling.

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