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SMITH & NEPHEW DYONICS INTELIJET REUSABLE CANNULAS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980092
510(k) Type
Traditional
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
3/9/1998
Days to Decision
59 days

SMITH & NEPHEW DYONICS INTELIJET REUSABLE CANNULAS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980092
510(k) Type
Traditional
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
3/9/1998
Days to Decision
59 days