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GENERAL PURPOSE ATL NEEDLE GUIDE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973958
510(k) Type
Traditional
Applicant
PROTEK MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1998
Days to Decision
98 days
Submission Type
Statement

GENERAL PURPOSE ATL NEEDLE GUIDE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973958
510(k) Type
Traditional
Applicant
PROTEK MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1998
Days to Decision
98 days
Submission Type
Statement