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ABI Instrument, Creo Electrosurgical System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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