Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000)
K-Number: K261068 · 2026-06-30
Device Summary
Frequently Asked Questions
What is the Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000)?
Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000) is a medical device that received FDA 510(k) clearance on 2026-06-30. The listed applicant is Serpex Medical. The 510(k) number is K261068.
When did Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000) receive FDA 510(k) clearance?
Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000) received FDA 510(k) clearance on 2026-06-30, under 510(k) number K261068.
Who is the listed applicant for Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000)?
The FDA 510(k) record lists Serpex Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000)?
The FDA product code for Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000) is GEH.
Other records listing Serpex Medical 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: GEH)
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.