CRYO-MONO CRYOGRNIC SYSTEM
K-Number: K991122 · 1999-07-01
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Device Summary
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.
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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