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EMAX 2 PLUS SYSTEM, MODEL EMAX 2 PLUS MOTOR, EMAX 2 CONSOLE>FIRMWARE UPGRADE, EMAX 2 FP FOOT PEDAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080802
510(k) Type
Special
Applicant
THE ANSPACH EFFORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2008
Days to Decision
40 days
Submission Type
Summary

EMAX 2 PLUS SYSTEM, MODEL EMAX 2 PLUS MOTOR, EMAX 2 CONSOLE>FIRMWARE UPGRADE, EMAX 2 FP FOOT PEDAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080802
510(k) Type
Special
Applicant
THE ANSPACH EFFORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2008
Days to Decision
40 days
Submission Type
Summary