FDA 510(k) FDA class 1 Substantially Equivalent 🇲🇬 Madagascar

PATIENT EXAMINATION LATEX GLOVES, HYPOALLERGENIC

K Number: K915251 · Decision Jan 22, 1993
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
9
Review Days
436

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
PATIENT EXAMINATION LATEX GLOVES, HYPOALLERGENIC
K Number
K915251
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Supermax Sdn Bhd
Date Received
November 13, 1991
Decision Date
January 22, 1993
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 Supermax Sdn Bhd

K Number Device Name
K013774 CHLORINATED POWDER FREE NITRILE MEDICAL EXAMINATION GLOVES WITH ALOE VERA
K993865 GREEN PEPPERMINT FLAVORED POWDERED LATEX EXAMINATION GLOVES
K993864 COLORED AND FLAVORED POWDER FREE LATEX EXAMINATION GLOVES
K993258 SUPERGLOVES, POWDER FREE NITRILE EXAMINATION GLOVES
K991415 SUPERGLOVES, POLYMER COATED POWDER FREE LATEX EXAMINATION GLOVES
K980966 SUPERGLOVES POWDERED NITRILE
K980494 SUPERGLOVES
K892287 PATIENT EXAMINATION GLOVES (LATEX)