FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

L3 (LEAD LATEX LYSNIG GLOVES)

K Number: K882437 · Decision May 11, 1989
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
78
Applicant Total
1
Review Days
331

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Basic Information

Device Name
L3 (LEAD LATEX LYSNIG GLOVES)
K Number
K882437
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
The Branford Co.
Date Received
June 14, 1988
Decision Date
May 11, 1989
Product Code
LZC
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
LZC Medical Glove, Specialty

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