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HAND TOOLS FOR ARTECH TYPE SS SUBMERGED SCREW IMPL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894160
510(k) Type
Traditional
Applicant
ARTECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1989
Days to Decision
106 days

HAND TOOLS FOR ARTECH TYPE SS SUBMERGED SCREW IMPL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894160
510(k) Type
Traditional
Applicant
ARTECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1989
Days to Decision
106 days