CRYOTRON-UL30
K-Number: K900419 · 1990-02-27
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Device Summary
Frequently Asked Questions
What is the CRYOTRON-UL30?
CRYOTRON-UL30 is a medical device that received FDA 510(k) clearance on 1990-02-27. The listed applicant is Henley Intl.. The 510(k) number is K900419.
When did CRYOTRON-UL30 receive FDA 510(k) clearance?
CRYOTRON-UL30 received FDA 510(k) clearance on 1990-02-27, under 510(k) number K900419.
Who is the listed applicant for CRYOTRON-UL30?
The FDA 510(k) record lists Henley Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRYOTRON-UL30?
The FDA product code for CRYOTRON-UL30 is IMF.
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 Henley Intl. 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: IMF)
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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