Last synced on 23 September 2022 at 11:05 pm

Keeogo Dermoskeleton System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201539
510(k) Type
Traditional
Applicant
B-Temia Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/9/2020
Days to Decision
92 days
Submission Type
Summary

Keeogo Dermoskeleton System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201539
510(k) Type
Traditional
Applicant
B-Temia Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/9/2020
Days to Decision
92 days
Submission Type
Summary