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

POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM

K Number: K990501 · Decision Apr 2, 1999
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
6
Review Days
44

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Basic Information

Device Name
POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM
K Number
K990501
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Flexitech Sdn. Bhd.
Date Received
February 17, 1999
Decision Date
April 2, 1999
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 Flexitech Sdn. Bhd.

K Number Device Name
K994416 POLYMER COATED POWDER FREE NITRILE EXAMINATION GLOVES, BLUE
K994354 POLYMER COATED, POWDER FREE, LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)
K990502 PREPOWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (100 MICROGRAMS OR LESS)
K990499 PREPOWDERED NITRILE EXAMINATION GLOVES
K990495 POWDER FREE NITRILE EXAMINATION GLOVES