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VERITAS Phacoemulsification Console, VERITAS Advanced Fluidics Pack and Advanced Infusion Pack, VERITAS Swivel Handpiece, VERITAS Advanced Foot Pedal, VERITAS Remote Control

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203060
510(k) Type
Traditional
Applicant
Johnson & Johnson Surgical Vision, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2021
Days to Decision
155 days
Submission Type
Summary

VERITAS Phacoemulsification Console, VERITAS Advanced Fluidics Pack and Advanced Infusion Pack, VERITAS Swivel Handpiece, VERITAS Advanced Foot Pedal, VERITAS Remote Control

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203060
510(k) Type
Traditional
Applicant
Johnson & Johnson Surgical Vision, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2021
Days to Decision
155 days
Submission Type
Summary