Last synced on 16 August 2024 at 11:05 pm

hekaDrill

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193630
510(k) Type
Traditional
Applicant
Zethon Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/9/2021
Days to Decision
470 days
Submission Type
Summary

hekaDrill

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193630
510(k) Type
Traditional
Applicant
Zethon Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/9/2021
Days to Decision
470 days
Submission Type
Summary