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

ROYAL SHIELD LATEX EXAMINATION GLOVES(TM)

K Number: K890907 · Decision Apr 26, 1989
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
5
Review Days
61

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Basic Information

Device Name
ROYAL SHIELD LATEX EXAMINATION GLOVES(TM)
K Number
K890907
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Shield Gloves Manufacturer Sdn. Bhd. C/O Lenty, Inc.
Date Received
February 24, 1989
Decision Date
April 26, 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 Shield Gloves Manufacturer Sdn. Bhd. C/O Lenty, Inc.

K Number Device Name
K952588 ROYAL SHIELD NON-STERILE LATEX EXAMINATION GLOVES
K952590 ROYAL SHIELD NON-STERILE PINK COLOERED, STRAWBERRY SCENTED LATEX EXAMINATION GLOVES
K952591 ROYAL SHIELD NON-STERILE BLUE COLORED BUBBLE GUM SCENTED LATEX EXAMINATION GLOVES
K926132 ROYAL SHIELD SHIELD GLOVES