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

PRE-POWDERED STERILE EXAM GLOVES

K Number: K052214 · Decision Sep 13, 2005
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
5
Review Days
29

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Basic Information

Device Name
PRE-POWDERED STERILE EXAM GLOVES
K Number
K052214
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kanam Latex Industries Pvt. , Ltd.
Date Received
August 15, 2005
Decision Date
September 13, 2005
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 Kanam Latex Industries Pvt. , Ltd.

K Number Device Name
K033564 POWDER FREE LATEX SURGEONS GLOVES POLYMER COATED STERILE WITH OPTIONAL LABELING CLAIM OF E.P. LESS THAN 50 UG/DM2
K013914 POWDERFREE LATEX SURGEON'S GLOVES
K904972 SURGICARE STERILE SURGICAL GLOVES
K897139 LATEX PATIENT EXAMINATION GLOVES