Patient Positioning System
K-Number: K170502 · 2017-04-13
ApplicantForte Automation Systems, Inc.
Decision Date2017-04-13
Product CodeJAI
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Patient Positioning System is a medical device manufactured by Forte Automation Systems, Inc.. It received FDA 510(k) clearance on 2017-04-13 under approval number K170502. The device is classified under product code JAI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Patient Positioning System?
Patient Positioning System is a medical device that received FDA 510(k) clearance on 2017-04-13. It is manufactured by Forte Automation Systems, Inc.. The 510(k) number is K170502.
When was Patient Positioning System approved by the FDA?
Patient Positioning System received FDA 510(k) clearance on 2017-04-13, under approval number K170502.
What company makes Patient Positioning System?
Patient Positioning System is manufactured by Forte Automation Systems, Inc..
What is the FDA product code for Patient Positioning System?
The FDA product code for Patient Positioning System is JAI.
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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.