FDA 510(k) FDA class 1 Substantially Equivalent 🇲🇱 Mali

GLOVE SEAL, POWDER FREE LATEX EXAMINATION GLOVES

K Number: K934316 · Decision Mar 11, 1994
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
5
Review Days
191

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Basic Information

Device Name
GLOVE SEAL, POWDER FREE LATEX EXAMINATION GLOVES
K Number
K934316
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Contract Latex Dippers Sdn Bhd
Date Received
September 1, 1993
Decision Date
March 11, 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.

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Other Clearances by Contract Latex Dippers Sdn Bhd

K Number Device Name
K011012 POWDER FREE NITRILE EXAMINATION GLOVE
K983568 OSTAR D'PRO LATEX POWDERED EXAMINATION GLOVES, PROTEIN CLAIM OF 100 MCGM OR/LESS OF TOTAL WATER EXTRACTABLE PROTEIN PER
K955947 OSTAR EXAMINATION GLOVES
K954063 GLOVE SEAL & SET-RITE