Last synced on 20 June 2025 at 11:06 pm

CLINI-LASE SYSTEM, MODELS CL-BASE, CL-2000, CL-1200, CL-500, CL-300, CL-275, CL-155, CL-55, CLP-BASE, CLP-275, CLP-55.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052647
510(k) Type
Traditional
Applicant
AMERICAN SPINE CENTER, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2005
Days to Decision
44 days
Submission Type
Summary

CLINI-LASE SYSTEM, MODELS CL-BASE, CL-2000, CL-1200, CL-500, CL-300, CL-275, CL-155, CL-55, CLP-BASE, CLP-275, CLP-55.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052647
510(k) Type
Traditional
Applicant
AMERICAN SPINE CENTER, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2005
Days to Decision
44 days
Submission Type
Summary