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SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010598
510(k) Type
Traditional
Applicant
Quantimetrix Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2001
Days to Decision
23 days
Submission Type
Summary

SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010598
510(k) Type
Traditional
Applicant
Quantimetrix Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2001
Days to Decision
23 days
Submission Type
Summary