510(k) K023627

ESSEX ENDOSCOPE, MODEL SXD-1000 by Guidant Corp. — Product Code GCJ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 12, 2002
Date Received
October 28, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
Laparoscope, General & Plastic Surgery
Device Class
Class II
Regulation Number
876.1500
Review Panel
SU
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).