FDA 510(k) FDA class 1 Substantially Equivalent 🇲🇾 Malaysia

POWDER-FREE LATEX PATIENT EXAMINATION GLOVES

K Number: K931633 · Decision Oct 25, 1993
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
5
Review Days
206

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Basic Information

Device Name
POWDER-FREE LATEX PATIENT EXAMINATION GLOVES
K Number
K931633
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tomarc (M) Sdn Bhd
Date Received
April 2, 1993
Decision Date
October 25, 1993
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 Tomarc (M) Sdn Bhd

K Number Device Name
K923589 STERILE HYPOALLERGENIC POWDER-FREE LATEX SURG. GLV
K892899 STERILE LATEX SURGICAL GLOVE
K890440 LATEX DECONTAMINATION/PROCEDURE GLOVES (NON-STER)
K890344 GLOVES, PATIENT EXAMINATION