CRYOMEDICS LLETZ LOOPS
K-Number: K923570 · 1994-02-28
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Device Summary
Frequently Asked Questions
What is the CRYOMEDICS LLETZ LOOPS?
CRYOMEDICS LLETZ LOOPS is a medical device that received FDA 510(k) clearance on 1994-02-28. The listed applicant is Cabot Medical Corp.. The 510(k) number is K923570.
When did CRYOMEDICS LLETZ LOOPS receive FDA 510(k) clearance?
CRYOMEDICS LLETZ LOOPS received FDA 510(k) clearance on 1994-02-28, under 510(k) number K923570.
Who is the listed applicant for CRYOMEDICS LLETZ LOOPS?
The FDA 510(k) record lists Cabot Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRYOMEDICS LLETZ LOOPS?
The FDA product code for CRYOMEDICS LLETZ LOOPS is HGI.
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 Cabot Medical Corp. 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: HGI)
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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