Last synced on 25 January 2026 at 3:41 am

SUPER NOVA, ACUBEAM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001179
510(k) Type
Traditional
Applicant
Light Force Therapy, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2000
Days to Decision
199 days
Submission Type
Statement

SUPER NOVA, ACUBEAM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001179
510(k) Type
Traditional
Applicant
Light Force Therapy, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2000
Days to Decision
199 days
Submission Type
Statement