Instrument kits
K-Number: K160730 · 2017-04-27
ApplicantAnthogyr
Decision Date2017-04-27
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Instrument kits is a medical device manufactured by Anthogyr. It received FDA 510(k) clearance on 2017-04-27 under approval number K160730. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Instrument kits?
Instrument kits is a medical device that received FDA 510(k) clearance on 2017-04-27. It is manufactured by Anthogyr. The 510(k) number is K160730.
When was Instrument kits approved by the FDA?
Instrument kits received FDA 510(k) clearance on 2017-04-27, under approval number K160730.
What company makes Instrument kits?
Instrument kits is manufactured by Anthogyr.
What is the FDA product code for Instrument kits?
The FDA product code for Instrument kits is KCT.
Other Devices by Anthogyr
Related Devices (Code: KCT)
K160574K3PRO SURGICAL TRAYArgon Med. Productions Vertriebs Gesellschaft Mbh CO KG
K162600Jewel Precision Reusable Rigid Sterilization Container SystemJewel Precision Sheet Metal & Machine, Inc.
K160912Sterilization TraySTERIS Corporation
K161347Signia sterilization trayCovidien
K152745ReNew Sterilization Trays(Catalog #3708 and #3709)Microline Surgical, Inc.
K152111Symmetry Surgical Quad-Lock Container SystemSymmetry Surgical, Inc.
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.