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

STERILE POWDERED LATEX PATIENT EXAMINATION GLOVES

K Number: K023915 · Decision Feb 11, 2003
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
4
Review Days
78

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Basic Information

Device Name
STERILE POWDERED LATEX PATIENT EXAMINATION GLOVES
K Number
K023915
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sanrea Healthcare Private Limited
Date Received
November 25, 2002
Decision Date
February 11, 2003
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 Sanrea Healthcare Private Limited

K Number Device Name
K023910 STERILE PATIENT POWDERFREE LATEX EXAMINATION GLOVES
K023912 POWDER FREE LATEX SURGEON'S GLOVES CONTAINS 50 MEGM OR LESS OF TOTAL WATER EXTRACTABLE PER GRAM
K023515 PRE-POWDERED LATEX SURGEON'S GLOVES