Last synced on 25 January 2026 at 3:41 am

ACCU-PULSE CARBON DIOXIDE LASER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971830
510(k) Type
Traditional
Applicant
Argus Photonics Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/1997
Days to Decision
90 days
Submission Type
Summary

ACCU-PULSE CARBON DIOXIDE LASER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971830
510(k) Type
Traditional
Applicant
Argus Photonics Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/1997
Days to Decision
90 days
Submission Type
Summary