510(k) K031648

VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V by Olympus Optical Co., Ltd. — Product Code EOB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 24, 2003
Date Received
May 28, 2003
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nasopharyngoscope (Flexible Or Rigid)
Device Class
Class II
Regulation Number
874.4760
Review Panel
EN
Submission Type

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).