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MODIFICATION TO ATRIUM MEDICAL CORPORATION CLEARWAY PTFE BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K020634
510(k) Type
Special
Applicant
Atrium Medical Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2002
Days to Decision
70 days
Submission Type
Statement

MODIFICATION TO ATRIUM MEDICAL CORPORATION CLEARWAY PTFE BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K020634
510(k) Type
Special
Applicant
Atrium Medical Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2002
Days to Decision
70 days
Submission Type
Statement