Last synced on 20 January 2023 at 11:05 pm

Benesta Hysteroscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192822
510(k) Type
Traditional
Applicant
Caldera Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2020
Days to Decision
344 days
Submission Type
Statement

Benesta Hysteroscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192822
510(k) Type
Traditional
Applicant
Caldera Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2020
Days to Decision
344 days
Submission Type
Statement