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KLEENSPEC SINGLE USE VAGINAL SPECULUM AND 790 SERIES CORDLESS ILLUMINATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070964
510(k) Type
Special
Applicant
WELCH ALLYN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2007
Days to Decision
43 days
Submission Type
Summary

KLEENSPEC SINGLE USE VAGINAL SPECULUM AND 790 SERIES CORDLESS ILLUMINATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070964
510(k) Type
Special
Applicant
WELCH ALLYN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2007
Days to Decision
43 days
Submission Type
Summary