CRYOMEDICS 5000 CRYOPROBES
K-Number: K832140 · 1983-08-12
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Device Summary
Frequently Asked Questions
What is the CRYOMEDICS 5000 CRYOPROBES?
CRYOMEDICS 5000 CRYOPROBES is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Spembly Medical , Ltd.. The 510(k) number is K832140.
When did CRYOMEDICS 5000 CRYOPROBES receive FDA 510(k) clearance?
CRYOMEDICS 5000 CRYOPROBES received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832140.
Who is the listed applicant for CRYOMEDICS 5000 CRYOPROBES?
The FDA 510(k) record lists Spembly Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRYOMEDICS 5000 CRYOPROBES?
The FDA product code for CRYOMEDICS 5000 CRYOPROBES 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 Spembly Medical , Ltd. 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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