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PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992174
510(k) Type
Traditional
Applicant
Pilling Weck Surgical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2000
Days to Decision
269 days
Submission Type
Statement

PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992174
510(k) Type
Traditional
Applicant
Pilling Weck Surgical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2000
Days to Decision
269 days
Submission Type
Statement