FDA 510(k) FDA class 1 Substantially Equivalent 🇮🇩 Indonesia

LATEX EXAMINATION GLOVES, POWDER FREE

K Number: K970977 · Decision Jun 27, 1997
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
3
Review Days
105

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Basic Information

Device Name
LATEX EXAMINATION GLOVES, POWDER FREE
K Number
K970977
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Arista Medi Prima
Date Received
March 14, 1997
Decision Date
June 27, 1997
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 Arista Medi Prima

K Number Device Name
K964629 VINYL PATIENT EXAMINATION GLOVES
K963742 LATEX EXAMINATION GLOVES, POWDERED