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

ALADAN STERILE LATEX MEDICAL GLOVE

K Number: K890880 · Decision Mar 29, 1989
Classifications
1
FEI Numbers
169
Registration Numbers
169
Same Product Code
1953
Applicant Total
18
Review Days
36

Basic Information

Device Name
ALADAN STERILE LATEX MEDICAL GLOVE
K Number
K890880
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
ALADAN CORP.
Date Received
February 21, 1989
Decision Date
March 29, 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

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Other Clearances by ALADAN CORP.

K Number Device Name
K960590 TRI-CLEAN 110/TRI-CLEAN PLUS GLOVE
K952404 SAFETEX SUPER HYPERALLERGENIC POWDERFREE LATEX MEDICAL GLOVE
K952556 SAFETEX SUPER HYPOALLERGENIC POWDERED LATEX EXAMINATION GLOVE
K943933 SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM
K951839 ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES
K943883 SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM
K942758 HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE
K940873 SAFETEX HYPOALLERGENIC POWDERFREE LATEX EXAMINATION GLOVE
K911774 ALADAN LATEX MEDICAL GLOVE
K911447 LATEX EXAMINATION GLOVES (HYPOALLERGENIC)
Search all 18 clearances from ALADAN CORP. →