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FDA 510(k)

SECCA SYSTEM

K-Number: K014216 · 2002-03-21

ApplicantCuron Medical, Inc.
Decision Date2002-03-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SECCA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Curon Medical, Inc.. It received FDA 510(k) clearance on 2002-03-21 under 510(k) number K014216. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECCA SYSTEM?

SECCA SYSTEM is a medical device that received FDA 510(k) clearance on 2002-03-21. The listed applicant is Curon Medical, Inc.. The 510(k) number is K014216.

When did SECCA SYSTEM receive FDA 510(k) clearance?

SECCA SYSTEM received FDA 510(k) clearance on 2002-03-21, under 510(k) number K014216.

Who is the listed applicant for SECCA SYSTEM?

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

What is the FDA product code for SECCA SYSTEM?

The FDA product code for SECCA SYSTEM is GEI.

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Other records listing Curon Medical, 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.

K010210CONTROL MODULE ALGORITHM ENHANCEMENT FOR THE MODEL S500-ST AND MODEL S400K002898CURON CONTROL MODULE ELECTROSURGICAL GENERATOR AND ACCESSORIES, MODEL S500-ST

Related Devices (Code: GEI)

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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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