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FDA 510(k)

CRYOSURGICAL PROBE

K-Number: K871314 · 1987-04-28

ApplicantWestern Medical Research
Decision Date1987-04-28
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CRYOSURGICAL PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Western Medical Research. It received FDA 510(k) clearance on 1987-04-28 under 510(k) number K871314. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRYOSURGICAL PROBE?

CRYOSURGICAL PROBE is a medical device that received FDA 510(k) clearance on 1987-04-28. The listed applicant is Western Medical Research. The 510(k) number is K871314.

When did CRYOSURGICAL PROBE receive FDA 510(k) clearance?

CRYOSURGICAL PROBE received FDA 510(k) clearance on 1987-04-28, under 510(k) number K871314.

Who is the listed applicant for CRYOSURGICAL PROBE?

The FDA 510(k) record lists Western Medical Research as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRYOSURGICAL PROBE?

The FDA product code for CRYOSURGICAL PROBE is GEH.

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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.

K262420Maverix Cryo Biopsy Pro (MCB Pro) (MCBP-1000); Maverix Cryo Cartridge (CC-1000)Serpex MedicalK261068Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000)Serpex MedicalK261806ERBECRYO 2 Cryosurgical Unit and AccessoriesErbe Elektromedizin GmbHK253230ERBECRYO 2 Cryosurgical Unit and Accessories: ERBECRYO 2 cryosurgical unit; Erbe Flexible CryoprobeErbe Elektromedizin GmbHK252198Advanced Cryo Skin Tag Remover (Advanced Skin Tag Remover)Medical Brands Laboratories B.V.K260377XSense Cryoablation System with CryoProbesIceCure Medical , Ltd.

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.

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