Last synced on 25 April 2025 at 11:05 pm

SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVE SuperPulsed Laser Fibers, and Accessories

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221306
510(k) Type
Traditional
Applicant
Gyrus ACMI, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2023
Days to Decision
267 days
Submission Type
Summary

SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVE SuperPulsed Laser Fibers, and Accessories

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221306
510(k) Type
Traditional
Applicant
Gyrus ACMI, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2023
Days to Decision
267 days
Submission Type
Summary