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

ALATECH POWDERED LATEX PATIENT EXAMINATION GLOVE

K Number: K080606 · Decision Aug 7, 2008
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
4
Review Days
156

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Basic Information

Device Name
ALATECH POWDERED LATEX PATIENT EXAMINATION GLOVE
K Number
K080606
Device Class
FDA class 1
Clearance Type
Abbreviated
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alatech Healthcare, LLC
Date Received
March 4, 2008
Decision Date
August 7, 2008
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 Alatech Healthcare, LLC

K Number Device Name
K083761 ALATECH POWDER FREE LATEX EXAMINATION GLOVE
K082529 ALATECH CHAMPION VYTEX LUBRICATED MALE LATEX CONDOM
K993887 ALATECH LATEX CONDOM