Last synced on 30 November 2024 at 11:09 am

hekaDrill

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233958
510(k) Type
Traditional
Applicant
Zethon Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/14/2024
Days to Decision
90 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
K233958
510(k) Type
Traditional
Applicant
Zethon Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/14/2024
Days to Decision
90 days
Submission Type
Summary