Last synced on 2 May 2025 at 11:05 pm

ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100266
510(k) Type
Abbreviated
Applicant
CAMNTECH, LTD
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/29/2010
Days to Decision
90 days
Submission Type
Summary

ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100266
510(k) Type
Abbreviated
Applicant
CAMNTECH, LTD
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/29/2010
Days to Decision
90 days
Submission Type
Summary