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FDA 510(k)

Instrument kits

K-Number: K160730 · 2017-04-27

ApplicantAnthogyr
Decision Date2017-04-27
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Instrument kits is the device name listed in this FDA 510(k) record. The listed applicant is Anthogyr. It received FDA 510(k) clearance on 2017-04-27 under 510(k) 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. 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

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