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ACCU-PULSE 1000 CO2 SURGICAL LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983543
510(k) Type
Traditional
Applicant
ARGUS PHOTONICS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1998
Days to Decision
68 days
Submission Type
Summary

ACCU-PULSE 1000 CO2 SURGICAL LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983543
510(k) Type
Traditional
Applicant
ARGUS PHOTONICS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1998
Days to Decision
68 days
Submission Type
Summary