FDA 510(k)

CDB CLIP

K-Number: K080906 · 2008-10-17

Decision Date2008-10-17

Product CodeNJM

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

CDB CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Cdb Corporation. It received FDA 510(k) clearance on 2008-10-17 under 510(k) number K080906. The device is classified under product code NJM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CDB CLIP?

CDB CLIP is a medical device that received FDA 510(k) clearance on 2008-10-17. The listed applicant is Cdb Corporation. The 510(k) number is K080906.

When did CDB CLIP receive FDA 510(k) clearance?

CDB CLIP received FDA 510(k) clearance on 2008-10-17, under 510(k) number K080906.

Who is the listed applicant for CDB CLIP?

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

What is the FDA product code for CDB CLIP?

The FDA product code for CDB CLIP is NJM.

Other records listing Cdb Corporation 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.

K212173HDH Treatment Planning System K210613HIT Clear Aligner K191823Clear-Aligners K160957CDB Self Ligating Bracket 8F K091702CDB FLIP-SIDE-CLIP BRACKET

Related Devices (Code: NJM)

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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.