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ABI Instrument, Creo Electrosurgical System

Page Type
Cleared 510(K)
510(k) Number
K200298
510(k) Type
Traditional
Applicant
Creo Medical Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/5/2021
Days to Decision
334 days
Submission Type
Summary

ABI Instrument, Creo Electrosurgical System

Page Type
Cleared 510(K)
510(k) Number
K200298
510(k) Type
Traditional
Applicant
Creo Medical Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/5/2021
Days to Decision
334 days
Submission Type
Summary