Last synced on 14 November 2025 at 11:06 pm

Zyter RPM

Page Type
Cleared 510(K)
510(k) Number
K212622
510(k) Type
Traditional
Applicant
Zyter, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2022
Days to Decision
177 days
Submission Type
Summary

Zyter RPM

Page Type
Cleared 510(K)
510(k) Number
K212622
510(k) Type
Traditional
Applicant
Zyter, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2022
Days to Decision
177 days
Submission Type
Summary