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

ACRYLIC DIPPED LATEX EXAMINATION GLOVES - STERILE

K Number: K945504 · Decision Aug 18, 1995
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
4
Review Days
282

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Basic Information

Device Name
ACRYLIC DIPPED LATEX EXAMINATION GLOVES - STERILE
K Number
K945504
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ganz Industries Sdn. Bhd.
Date Received
November 9, 1994
Decision Date
August 18, 1995
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.

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Other Clearances by Ganz Industries Sdn. Bhd.

K Number Device Name
K954487 PRE POWDERED LATEX EXAMINATION GLOVES
K945506 ACRYLIC DIPPED LATEX EXAMINATION GLOVES
K945505 ACRYLIC DIPPED LATEX SURGICAL GLOVES - STERILE