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GOLDWAY DIGITAL VIDEO COLPOSCOPE IMAGING SYSTEM, MODEL #SLC-2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021153
510(k) Type
Traditional
Applicant
GOLDWAY US, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2003
Days to Decision
306 days
Submission Type
Summary

GOLDWAY DIGITAL VIDEO COLPOSCOPE IMAGING SYSTEM, MODEL #SLC-2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021153
510(k) Type
Traditional
Applicant
GOLDWAY US, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2003
Days to Decision
306 days
Submission Type
Summary