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

HPI POWDER FREE NON-STERILE EXAMINATION GLOVES

K Number: K901608 · Decision Apr 20, 1990
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
6
Review Days
14

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Basic Information

Device Name
HPI POWDER FREE NON-STERILE EXAMINATION GLOVES
K Number
K901608
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Hpi, Inc.
Date Received
April 6, 1990
Decision Date
April 20, 1990
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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K Number Device Name
K922116 POWDER FREE NITRILE GLOVE
K915086 HPI BROWN NITRILE SENSI-GRIP SURGICAL GLOVES
K910383 HPI SENSI-SHIELD GLOVE KIT
K904878 SENSI RADS LEAD LATEX RADIATION PROT. GLOVE, STER.
K905086 HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES