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MEDIWORKS SLIT LAMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100439
510(k) Type
Traditional
Applicant
SHANGHAI MEDIWORKS PRECISION INSTRUMENTS CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2010
Days to Decision
149 days
Submission Type
Statement

MEDIWORKS SLIT LAMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100439
510(k) Type
Traditional
Applicant
SHANGHAI MEDIWORKS PRECISION INSTRUMENTS CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2010
Days to Decision
149 days
Submission Type
Statement