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

PERRY(R) CUT-RESISTANT GLOVES

K Number: K914942 · Decision Jan 31, 1992
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
10
Review Days
88

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Basic Information

Device Name
PERRY(R) CUT-RESISTANT GLOVES
K Number
K914942
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Smith & Nephew Perry
Date Received
November 4, 1991
Decision Date
January 31, 1992
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

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Other Clearances by Smith & Nephew Perry

K Number Device Name
K932665 ENCORE POWDER-FREE SURGICAL GLOVES MICROPTIC
K932664 ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA
K931399 PERRY ENHANCED PROTECTION LATEX SURGICAL GLOVE
K923929 PERRY POWDER-FREE GLOVES, STYLE 45G
K922379 STERILE LATEX EXAMINATION GLOVES
K914445 PERRY(R) NATURAL POWDER-FREE GLOVES, STYLE 45
K913402 PERRY(R) DERMAGUARD(R) PLUS GLOVES
K911633 PERRY(R) ENCORE CHEMOTHERAPY GLOVE
K905537 PERRY XTENDA CUFF SURGICAL GLOVES