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FDA 510(k)

CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12

K-Number: K041890 · 2004-09-22

ApplicantCryocor, Inc.
Decision Date2004-09-22
Product CodeOCL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12 is the device name listed in this FDA 510(k) record. The listed applicant is Cryocor, Inc.. It received FDA 510(k) clearance on 2004-09-22 under 510(k) number K041890. The device is classified under product code OCL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12?

CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12 is a medical device that received FDA 510(k) clearance on 2004-09-22. The listed applicant is Cryocor, Inc.. The 510(k) number is K041890.

When did CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12 receive FDA 510(k) clearance?

CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12 received FDA 510(k) clearance on 2004-09-22, under 510(k) number K041890.

Who is the listed applicant for CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12?

The FDA 510(k) record lists Cryocor, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12?

The FDA product code for CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12 is OCL.

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Other records listing Cryocor, 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.

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Related Devices (Code: OCL)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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