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EPXPRESS SYSTEM (TIMBERWOLF REVISION) /000391

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971570
510(k) Type
Traditional
Applicant
Quinton Electrophysiology Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1997
Days to Decision
244 days
Submission Type
Summary

EPXPRESS SYSTEM (TIMBERWOLF REVISION) /000391

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971570
510(k) Type
Traditional
Applicant
Quinton Electrophysiology Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1997
Days to Decision
244 days
Submission Type
Summary