ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM
K-Number: K980110 · 1998-04-10
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Device Summary
Frequently Asked Questions
What is the ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM?
ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM is a medical device that received FDA 510(k) clearance on 1998-04-10. The listed applicant is Endocare, Inc.. The 510(k) number is K980110.
When did ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM receive FDA 510(k) clearance?
ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM received FDA 510(k) clearance on 1998-04-10, under 510(k) number K980110.
Who is the listed applicant for ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM?
The FDA 510(k) record lists Endocare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM?
The FDA product code for ENDOCRE CRYOCARE CRYOSURGICAL 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 Endocare, 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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