Last synced on 25 November 2022 at 11:04 pm

HAYMAX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120894
510(k) Type
Traditional
Applicant
HAYMAX LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/17/2012
Days to Decision
55 days
Submission Type
Summary