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GENERAL PURPOSE ATL NEEDLE GUIDE KIT

Page Type
Cleared 510(K)
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)
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