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POLYETHYLENE MONITORING CONNECTORS

Page Type
Cleared 510(K)
510(k) Number
K830420
510(k) Type
Traditional
Applicant
VERTEX MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1983
Days to Decision
20 days

POLYETHYLENE MONITORING CONNECTORS

Page Type
Cleared 510(K)
510(k) Number
K830420
510(k) Type
Traditional
Applicant
VERTEX MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1983
Days to Decision
20 days