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

POWDERFREE LATEX SURGEON'S GLOVES WITH PROTIEN LABELING CLAIM (50 MOCROGRAMS OR LESS

K Number: K000896 · Decision May 3, 2000
Classifications
1
FEI Numbers
138
Registration Numbers
138
Same Product Code
558
Applicant Total
6
Review Days
44

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Basic Information

Device Name
POWDERFREE LATEX SURGEON'S GLOVES WITH PROTIEN LABELING CLAIM (50 MOCROGRAMS OR LESS
K Number
K000896
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4460
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Fitco Dipped Products Pvt., Ltd.
Date Received
March 20, 2000
Decision Date
May 3, 2000
Product Code
KGO
Advisory Committee
General, Plastic Surgery
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
KGO Surgeon'S Gloves

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KGO), ordered by most recent decision date.

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Other Clearances by Fitco Dipped Products Pvt., Ltd.

K Number Device Name
K001715 POWDERED PATIENT EXAMINATION GLOVES, LATEX
K001232 NON-STERILE POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM 50 MICROGRAMS OR LESS
K001216 POWDER-FREE LATEX EXAMINATION GLOVE STERILE WITH OPTIONAL PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS)
K000891 STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES
K993450 LATEX SURGICAL GLOVES, PRE-POWDERED