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SMITH & NEPHEW MIS INSTRUMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970949
510(k) Type
Traditional
Applicant
SMITH & NEPHEW ENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/1997
Days to Decision
40 days
Submission Type
Summary