Instrument kits
K-Number: K160730 · 2017-04-27
Device Summary
Frequently Asked Questions
What is the Instrument kits?
Instrument kits is a medical device that received FDA 510(k) clearance on 2017-04-27. The listed applicant is Anthogyr. The 510(k) number is K160730.
When did Instrument kits receive FDA 510(k) clearance?
Instrument kits received FDA 510(k) clearance on 2017-04-27, under 510(k) number K160730.
Who is the listed applicant for Instrument kits?
The FDA 510(k) record lists Anthogyr as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Instrument kits?
The FDA product code for Instrument kits is KCT.
Other records listing Anthogyr as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KCT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.