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FDA 510(k)

DIVE AND SHALLOW AND GRAND DIVE

K-Number: K072757 · 2008-02-08

ApplicantSummit TO Sea
Decision Date2008-02-08
Product CodeCBF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DIVE AND SHALLOW AND GRAND DIVE is the device name listed in this FDA 510(k) record. The listed applicant is Summit TO Sea. It received FDA 510(k) clearance on 2008-02-08 under 510(k) number K072757. The device is classified under product code CBF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIVE AND SHALLOW AND GRAND DIVE?

DIVE AND SHALLOW AND GRAND DIVE is a medical device that received FDA 510(k) clearance on 2008-02-08. The listed applicant is Summit TO Sea. The 510(k) number is K072757.

When did DIVE AND SHALLOW AND GRAND DIVE receive FDA 510(k) clearance?

DIVE AND SHALLOW AND GRAND DIVE received FDA 510(k) clearance on 2008-02-08, under 510(k) number K072757.

Who is the listed applicant for DIVE AND SHALLOW AND GRAND DIVE?

The FDA 510(k) record lists Summit TO Sea as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIVE AND SHALLOW AND GRAND DIVE?

The FDA product code for DIVE AND SHALLOW AND GRAND DIVE is CBF.

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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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