Last synced on 2 December 2022 at 11:04 pm

SINGLE USE SPLINTING TUBE, MODELS ST-Y0002-S, ST-Y0002-H, ST-Y0003-S AND ST-Y0003-H

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091759
510(k) Type
Traditional
Applicant
OLYMPUS MEDICAL SYSTEMS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2009
Days to Decision
94 days
Submission Type
Summary