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STERILS SINGLE-USE I/A HANDPIECES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073023
510(k) Type
Special
Applicant
BAUSCH & LOMB, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2008
Days to Decision
138 days
Submission Type
Summary

STERILS SINGLE-USE I/A HANDPIECES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073023
510(k) Type
Special
Applicant
BAUSCH & LOMB, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2008
Days to Decision
138 days
Submission Type
Summary