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FDA 510(k)

LIQUID NITROGEN SPRAY UNIT

K-Number: K772232 · 1977-12-15

ApplicantGilmore Liquid Air Co.
Decision Date1977-12-15
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIQUID NITROGEN SPRAY UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Gilmore Liquid Air Co.. It received FDA 510(k) clearance on 1977-12-15 under 510(k) number K772232. 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 LIQUID NITROGEN SPRAY UNIT?

LIQUID NITROGEN SPRAY UNIT is a medical device that received FDA 510(k) clearance on 1977-12-15. The listed applicant is Gilmore Liquid Air Co.. The 510(k) number is K772232.

When did LIQUID NITROGEN SPRAY UNIT receive FDA 510(k) clearance?

LIQUID NITROGEN SPRAY UNIT received FDA 510(k) clearance on 1977-12-15, under 510(k) number K772232.

Who is the listed applicant for LIQUID NITROGEN SPRAY UNIT?

The FDA 510(k) record lists Gilmore Liquid Air Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUID NITROGEN SPRAY UNIT?

The FDA product code for LIQUID NITROGEN SPRAY UNIT is GEH.

Related Clinical Trials

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.

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Other records listing Gilmore Liquid Air Co. 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.

K801921GCS-79

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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