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FDA 510(k)

EXICLIP EXCS-M

K-Number: K070836 · 2007-04-20

ApplicantClevex, Inc.
Decision Date2007-04-20
Product CodeMJG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EXICLIP EXCS-M is the device name listed in this FDA 510(k) record. The listed applicant is Clevex, Inc.. It received FDA 510(k) clearance on 2007-04-20 under 510(k) number K070836. The device is classified under product code MJG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXICLIP EXCS-M?

EXICLIP EXCS-M is a medical device that received FDA 510(k) clearance on 2007-04-20. The listed applicant is Clevex, Inc.. The 510(k) number is K070836.

When did EXICLIP EXCS-M receive FDA 510(k) clearance?

EXICLIP EXCS-M received FDA 510(k) clearance on 2007-04-20, under 510(k) number K070836.

Who is the listed applicant for EXICLIP EXCS-M?

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

What is the FDA product code for EXICLIP EXCS-M?

The FDA product code for EXICLIP EXCS-M is MJG.

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Related Devices (Code: MJG)

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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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