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BenestaTM Tissue Removal Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192811
510(k) Type
Traditional
Applicant
Caldera Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2020
Days to Decision
389 days
Submission Type
Statement

BenestaTM Tissue Removal Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192811
510(k) Type
Traditional
Applicant
Caldera Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2020
Days to Decision
389 days
Submission Type
Statement