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FDA 510(k)

RESILIENCE M5 PROTECTION PLUS

K-Number: K955329 · 1996-03-28

Decision Date1996-03-28
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RESILIENCE M5 PROTECTION PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Confi-Dental Products Co.. It received FDA 510(k) clearance on 1996-03-28 under 510(k) number K955329. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESILIENCE M5 PROTECTION PLUS?

RESILIENCE M5 PROTECTION PLUS is a medical device that received FDA 510(k) clearance on 1996-03-28. The listed applicant is Confi-Dental Products Co.. The 510(k) number is K955329.

When did RESILIENCE M5 PROTECTION PLUS receive FDA 510(k) clearance?

RESILIENCE M5 PROTECTION PLUS received FDA 510(k) clearance on 1996-03-28, under 510(k) number K955329.

Who is the listed applicant for RESILIENCE M5 PROTECTION PLUS?

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

What is the FDA product code for RESILIENCE M5 PROTECTION PLUS?

The FDA product code for RESILIENCE M5 PROTECTION PLUS is DYH.

Related Clinical Trials

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.

Other records listing Confi-Dental Products Co. 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 31 devices →

Related Devices (Code: DYH)

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

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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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