FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LATEX EXAM GLOVE, POWDER-FREE W/PROTEIN & HYPOALLERGENIC LABELING

K Number: K973664 · Decision Mar 13, 1998
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
3
Review Days
169

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
LATEX EXAM GLOVE, POWDER-FREE W/PROTEIN & HYPOALLERGENIC LABELING
K Number
K973664
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Evergrade Healthcare Products Sdn Bhd
Date Received
September 25, 1997
Decision Date
March 13, 1998
Product Code
LYY
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LYY Latex Patient Examination Glove

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LYY), ordered by most recent decision date.

View all

Other Clearances by Evergrade Healthcare Products Sdn Bhd

K Number Device Name
K942855 NON-CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES
K932116 PATIENT EXAMINATION GLOVES (POWDER FREE)