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DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960400
510(k) Type
Traditional
Applicant
SNOWDEN-PENCER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1996
Days to Decision
43 days
Submission Type
Summary

DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960400
510(k) Type
Traditional
Applicant
SNOWDEN-PENCER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1996
Days to Decision
43 days
Submission Type
Summary