FDA 510(k) FDA class 1 Substantially Equivalent 🇲🇾 Malaysia

POWDER FREE LATEX EXAMINATION GLOVES

K Number: K935946 · Decision Jun 21, 1994
Classifications
1
FEI Numbers
169
Registration Numbers
169
Same Product Code
1953
Applicant Total
4
Review Days
190

Basic Information

Device Name
POWDER FREE LATEX EXAMINATION GLOVES
K Number
K935946
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
CRANBERRY (M) SDN. BHD.
Date Received
December 13, 1993
Decision Date
June 21, 1994
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 CRANBERRY (M) SDN. BHD.

K Number Device Name
K984039 CRANBERRY POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESSS)
K983334 NITRILE POWDER FREE EXAMINATION GLOVES
K890976 PATIENT EXAMINATION GLOVE