510(k) K132566

REPROCESSED HARMONIC SHEAR by Sterilmed, Inc. — Product Code NLQ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 14, 2014
Date Received
August 15, 2013
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Single-Use Reprocessed Ultrasonic Surgical Instruments
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type

Single-use reprocessed versions of the ultrasonic devices used in surgical procedures either for fragmentation, emulsification and aspiration of soft tissue and hard tissue or for ligation of vessels (under product code “LFL”). Reprocessing validation data for this device type must be included in a 510(k) submission.. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).