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Creo Electrosurgical System with NP1 Instrument

Page Type
Cleared 510(K)
510(k) Number
K221672
510(k) Type
Traditional
Applicant
Creo Medical Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/14/2023
Days to Decision
250 days
Submission Type
Summary

Creo Electrosurgical System with NP1 Instrument

Page Type
Cleared 510(K)
510(k) Number
K221672
510(k) Type
Traditional
Applicant
Creo Medical Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/14/2023
Days to Decision
250 days
Submission Type
Summary