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FDA 510(k)

CLP BONNET

K-Number: K955528 · 1996-02-14

ApplicantClp Products
Decision Date1996-02-14
Product CodeDZB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLP BONNET is the device name listed in this FDA 510(k) record. The listed applicant is Clp Products. It received FDA 510(k) clearance on 1996-02-14 under 510(k) number K955528. The device is classified under product code DZB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLP BONNET?

CLP BONNET is a medical device that received FDA 510(k) clearance on 1996-02-14. The listed applicant is Clp Products. The 510(k) number is K955528.

When did CLP BONNET receive FDA 510(k) clearance?

CLP BONNET received FDA 510(k) clearance on 1996-02-14, under 510(k) number K955528.

Who is the listed applicant for CLP BONNET?

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

What is the FDA product code for CLP BONNET?

The FDA product code for CLP BONNET is DZB.

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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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