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FDA 510(k)

FIBER FORCE

K-Number: K102207 · 2010-11-23

ApplicantSynca Marketing, Inc.
Decision Date2010-11-23
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIBER FORCE is the device name listed in this FDA 510(k) record. The listed applicant is Synca Marketing, Inc.. It received FDA 510(k) clearance on 2010-11-23 under 510(k) number K102207. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBER FORCE?

FIBER FORCE is a medical device that received FDA 510(k) clearance on 2010-11-23. The listed applicant is Synca Marketing, Inc.. The 510(k) number is K102207.

When did FIBER FORCE receive FDA 510(k) clearance?

FIBER FORCE received FDA 510(k) clearance on 2010-11-23, under 510(k) number K102207.

Who is the listed applicant for FIBER FORCE?

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

What is the FDA product code for FIBER FORCE?

The FDA product code for FIBER FORCE is EBI.

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.

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Other records listing Synca Marketing, 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.

K062237CADI, VERSION 4

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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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