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FDA 510(k)

DEEP BLUE

K-Number: K071722 · 2007-08-10

ApplicantE.M.S Electro Medical Systems S.A
Decision Date2007-08-10
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DEEP BLUE is the device name listed in this FDA 510(k) record. The listed applicant is E.M.S Electro Medical Systems S.A. It received FDA 510(k) clearance on 2007-08-10 under 510(k) number K071722. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEEP BLUE?

DEEP BLUE is a medical device that received FDA 510(k) clearance on 2007-08-10. The listed applicant is E.M.S Electro Medical Systems S.A. The 510(k) number is K071722.

When did DEEP BLUE receive FDA 510(k) clearance?

DEEP BLUE received FDA 510(k) clearance on 2007-08-10, under 510(k) number K071722.

Who is the listed applicant for DEEP BLUE?

The FDA 510(k) record lists E.M.S Electro Medical Systems S.A as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEEP BLUE?

The FDA product code for DEEP BLUE is EBZ.

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Related Devices (Code: EBZ)

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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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