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

NITRILE EXAMINATION GLOVES - POWDER FREE

K Number: K980511 · Decision Mar 13, 1998
Classifications
1
FEI Numbers
380
Registration Numbers
380
Same Product Code
1171
Applicant Total
5
Review Days
31

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
NITRILE EXAMINATION GLOVES - POWDER FREE
K Number
K980511
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Influx Pacific Sdn. Bhd.
Date Received
February 10, 1998
Decision Date
March 13, 1998
Product Code
LZA
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
LZA Polymer Patient Examination Glove

Similar 510(k) Clearances

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

View all

Other Clearances by Influx Pacific Sdn. Bhd.

K Number Device Name
K970216 NITRILE EXAMINATION GLOVES-PRE POWDERED
K930407 POWDER-FREE LATEX EXAMINATION GLOVES
K910895 SURGICAL GLOVES
K891668 PATIENT EXAMINATION GLOVES (LATEX)