Last synced on 17 January 2025 at 11:05 pm

Xenocor Articulating Xenoscope Laparoscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193315
510(k) Type
Special
Applicant
Xenocor, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2020
Days to Decision
59 days
Submission Type
Summary