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FDA 510(k)

CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU.

K-Number: K896724 · 1990-01-09

ApplicantStiefel Research Institute, Inc.
Decision Date1990-01-09
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU. is the device name listed in this FDA 510(k) record. The listed applicant is Stiefel Research Institute, Inc.. It received FDA 510(k) clearance on 1990-01-09 under 510(k) number K896724. 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 CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU.?

CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU. is a medical device that received FDA 510(k) clearance on 1990-01-09. The listed applicant is Stiefel Research Institute, Inc.. The 510(k) number is K896724.

When did CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU. receive FDA 510(k) clearance?

CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU. received FDA 510(k) clearance on 1990-01-09, under 510(k) number K896724.

Who is the listed applicant for CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU.?

The FDA 510(k) record lists Stiefel Research Institute, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU.?

The FDA product code for CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU. is GEH.

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Other records listing Stiefel Research Institute, Inc. as applicant

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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.

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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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