FDA 510(k) FDA class 1 Substantially Equivalent 🇹🇭 Thailand

PATIENT EXAMINATION GLOVES (LATEX)

K Number: K891326 · Decision Sep 13, 1989
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
6
Review Days
184

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Basic Information

Device Name
PATIENT EXAMINATION GLOVES (LATEX)
K Number
K891326
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Medigloves , Ltd.
Date Received
March 13, 1989
Decision Date
September 13, 1989
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 Medigloves , Ltd.

K Number Device Name
K050181 MEDIGLOVES STERILE POWDER-FREE SYNTHETIC POLYISOPRENE SURGICAL GLOVES
K930794 MEDIGLOVES, MEDPAC, BOSTON, FISHERBRAND, GLOVES
K930795 MEDIGLOVES, FISHERBRAND, MEDIPRODUCTS GLOVES
K912503 HYPOALLERGENIC EXAMINATION LATEX GLOVES
K912157 HYPOALLERGENIC SURGICAL LATEX GLOVES