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TRI-PLEX ADAPTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010401
510(k) Type
Traditional
Applicant
THE MEDICAL DEVICE GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2002
Days to Decision
625 days
Submission Type
Statement

TRI-PLEX ADAPTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010401
510(k) Type
Traditional
Applicant
THE MEDICAL DEVICE GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2002
Days to Decision
625 days
Submission Type
Statement