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BETA-PREG

Page Type
Cleared 510(K)
510(k) Number
K831361
510(k) Type
Traditional
Applicant
CATHETER TECHNOLOGY CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1983
Days to Decision
37 days

BETA-PREG

Page Type
Cleared 510(K)
510(k) Number
K831361
510(k) Type
Traditional
Applicant
CATHETER TECHNOLOGY CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1983
Days to Decision
37 days