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PAJUNK STANDARD SPROTTE NEEDLE W/ INTRODUCER CANN.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923003
510(k) Type
Traditional
Applicant
RUSCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1993
Days to Decision
297 days
Submission Type
Statement

PAJUNK STANDARD SPROTTE NEEDLE W/ INTRODUCER CANN.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923003
510(k) Type
Traditional
Applicant
RUSCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1993
Days to Decision
297 days
Submission Type
Statement