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CATHETER, MMG LATEX EXTERNAL

Page Type
Cleared 510(K)
510(k) Number
K790279
510(k) Type
Traditional
Applicant
MEDICAL MARKETING GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1979
Days to Decision
21 days

CATHETER, MMG LATEX EXTERNAL

Page Type
Cleared 510(K)
510(k) Number
K790279
510(k) Type
Traditional
Applicant
MEDICAL MARKETING GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1979
Days to Decision
21 days