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MAXGUARD ADVANCED LUER ACTIVATED DEVICE WITH ANTIMICROBIAL

Page Type
Cleared 510(K)
510(k) Number
K083765
510(k) Type
Traditional
Applicant
MEDEGEN MEDICAL MANUFACTURING SERVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2008
Days to Decision
12 days
Submission Type
Statement

MAXGUARD ADVANCED LUER ACTIVATED DEVICE WITH ANTIMICROBIAL

Page Type
Cleared 510(K)
510(k) Number
K083765
510(k) Type
Traditional
Applicant
MEDEGEN MEDICAL MANUFACTURING SERVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2008
Days to Decision
12 days
Submission Type
Statement