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HandX™ Self-Righting Needle Holder

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223718
510(k) Type
Traditional
Applicant
Human Xtensions Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
6/5/2023
Days to Decision
175 days
Submission Type
Summary