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SUNLITELED MODEL #2810

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012946
510(k) Type
Traditional
Applicant
Kinetic Instruments, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2001
Days to Decision
28 days
Submission Type
Statement

SUNLITELED MODEL #2810

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012946
510(k) Type
Traditional
Applicant
Kinetic Instruments, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2001
Days to Decision
28 days
Submission Type
Statement