FDA 510(k) FDA class 1 Substantially Equivalent 🇮🇳 India

POWDER FREE LATEX EXAM GLOVES

K Number: K925685 · Decision Jun 25, 1993
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
2
Review Days
225

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Basic Information

Device Name
POWDER FREE LATEX EXAM GLOVES
K Number
K925685
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
M.M. Rubber Co. , Ltd.
Date Received
November 12, 1992
Decision Date
June 25, 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.

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Other Clearances by M.M. Rubber Co. , Ltd.

K Number Device Name
K893357 LATEX EXAMINATION GLOVES