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Lifetech Cardio Model 8301 Temporary Pacemaker

Page Type
Cleared 510(K)
510(k) Number
K182839
510(k) Type
Traditional
Applicant
Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/28/2019
Days to Decision
142 days
Submission Type
Summary

Lifetech Cardio Model 8301 Temporary Pacemaker

Page Type
Cleared 510(K)
510(k) Number
K182839
510(k) Type
Traditional
Applicant
Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/28/2019
Days to Decision
142 days
Submission Type
Summary