510(k) K050580

SMITH & NEPHEW INTELIJET FLUID MANAGEMENT SYSTEMS by Smith & Nephew Endoscopy, Inc. — Product Code HRX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 20, 2005
Date Received
March 7, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Arthroscope
Device Class
Class II
Regulation Number
888.1100
Review Panel
OR
Submission Type

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).