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FDA 510(k)

CRYO-MONO CRYOGRNIC SYSTEM

K-Number: K991122 · 1999-07-01

Decision Date1999-07-01
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CRYO-MONO CRYOGRNIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Influence, Inc.. It received FDA 510(k) clearance on 1999-07-01 under 510(k) number K991122. 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 CRYO-MONO CRYOGRNIC SYSTEM?

CRYO-MONO CRYOGRNIC SYSTEM is a medical device that received FDA 510(k) clearance on 1999-07-01. The listed applicant is Influence, Inc.. The 510(k) number is K991122.

When did CRYO-MONO CRYOGRNIC SYSTEM receive FDA 510(k) clearance?

CRYO-MONO CRYOGRNIC SYSTEM received FDA 510(k) clearance on 1999-07-01, under 510(k) number K991122.

Who is the listed applicant for CRYO-MONO CRYOGRNIC SYSTEM?

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

What is the FDA product code for CRYO-MONO CRYOGRNIC SYSTEM?

The FDA product code for CRYO-MONO CRYOGRNIC SYSTEM 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.

Other records listing Influence, Inc. 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.

View all 16 devices →

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.

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