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FDA 510(k)

FLEX-STAR V

K-Number: K072402 · 2007-10-19

Decision Date2007-10-19
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLEX-STAR V is the device name listed in this FDA 510(k) record. The listed applicant is Cmp Industries, LLC. It received FDA 510(k) clearance on 2007-10-19 under 510(k) number K072402. 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 FLEX-STAR V?

FLEX-STAR V is a medical device that received FDA 510(k) clearance on 2007-10-19. The listed applicant is Cmp Industries, LLC. The 510(k) number is K072402.

When did FLEX-STAR V receive FDA 510(k) clearance?

FLEX-STAR V received FDA 510(k) clearance on 2007-10-19, under 510(k) number K072402.

Who is the listed applicant for FLEX-STAR V?

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

What is the FDA product code for FLEX-STAR V?

The FDA product code for FLEX-STAR V is EBI.

Other records listing Cmp Industries, LLC 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.

View all 7 devices →

Related Devices (Code: EBI)

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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