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ATRIUM'S HYBRID PTFE

Page Type
Cleared 510(K)
510(k) Number
K925123
510(k) Type
Traditional
Applicant
ATRIUM MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
5/27/1993
Days to Decision
226 days
Submission Type
Summary

ATRIUM'S HYBRID PTFE

Page Type
Cleared 510(K)
510(k) Number
K925123
510(k) Type
Traditional
Applicant
ATRIUM MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
5/27/1993
Days to Decision
226 days
Submission Type
Summary