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FDA 510(k)

Thermo Scientific Oxoid Cefepime/Zidebactam Disc (30/30 µg) FPZ60

K-Number: K261781 · 2026-07-24

Decision Date2026-07-24
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

Thermo Scientific Oxoid Cefepime/Zidebactam Disc (30/30 µg) FPZ60 is the device name listed in this FDA 510(k) record. The listed applicant is Thermo Fisher Scientific (Oxoid Ltd.). It received FDA 510(k) clearance on 2026-07-24 under 510(k) number K261781. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Thermo Scientific Oxoid Cefepime/Zidebactam Disc (30/30 µg) FPZ60?

Thermo Scientific Oxoid Cefepime/Zidebactam Disc (30/30 µg) FPZ60 is a medical device that received FDA 510(k) clearance on 2026-07-24. The listed applicant is Thermo Fisher Scientific (Oxoid Ltd.). The 510(k) number is K261781.

When did Thermo Scientific Oxoid Cefepime/Zidebactam Disc (30/30 µg) FPZ60 receive FDA 510(k) clearance?

Thermo Scientific Oxoid Cefepime/Zidebactam Disc (30/30 µg) FPZ60 received FDA 510(k) clearance on 2026-07-24, under 510(k) number K261781.

Who is the listed applicant for Thermo Scientific Oxoid Cefepime/Zidebactam Disc (30/30 µg) FPZ60?

The FDA 510(k) record lists Thermo Fisher Scientific (Oxoid Ltd.) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Thermo Scientific Oxoid Cefepime/Zidebactam Disc (30/30 µg) FPZ60?

The FDA product code for Thermo Scientific Oxoid Cefepime/Zidebactam Disc (30/30 µg) FPZ60 is JTN.

Other records listing Thermo Fisher Scientific (Oxoid Ltd.) 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: JTN)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.