SIS Software
K-Number: K162830 · 2017-02-14
ApplicantSurgical Information Sciences, Inc.
Decision Date2017-02-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
SIS Software is a medical device manufactured by Surgical Information Sciences, Inc.. It received FDA 510(k) clearance on 2017-02-14 under approval number K162830. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SIS Software?
SIS Software is a medical device that received FDA 510(k) clearance on 2017-02-14. It is manufactured by Surgical Information Sciences, Inc.. The 510(k) number is K162830.
When was SIS Software approved by the FDA?
SIS Software received FDA 510(k) clearance on 2017-02-14, under approval number K162830.
What company makes SIS Software?
SIS Software is manufactured by Surgical Information Sciences, Inc..
What is the FDA product code for SIS Software?
The FDA product code for SIS Software is LLZ.
Other Devices by Surgical Information Sciences, Inc.
Related Devices (Code: LLZ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.