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PILLING WECK SECONDARY FLEXIBLE SLEEVE WITH TROCAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971334
510(k) Type
Traditional
Applicant
PILLING WECK GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1997
Days to Decision
62 days
Submission Type
Summary