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Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192867
510(k) Type
Traditional
Applicant
Bovie Medical Corporation dba Apyx Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2019
Days to Decision
24 days
Submission Type
Summary

Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192867
510(k) Type
Traditional
Applicant
Bovie Medical Corporation dba Apyx Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2019
Days to Decision
24 days
Submission Type
Summary