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FDA 510(k)

PRECIMED TRAUMA SYSTEM

K-Number: K002486 · 2000-11-09

ApplicantPatrick Berdoz
Decision Date2000-11-09
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PRECIMED TRAUMA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Patrick Berdoz. It received FDA 510(k) clearance on 2000-11-09 under 510(k) number K002486. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECIMED TRAUMA SYSTEM?

PRECIMED TRAUMA SYSTEM is a medical device that received FDA 510(k) clearance on 2000-11-09. The listed applicant is Patrick Berdoz. The 510(k) number is K002486.

When did PRECIMED TRAUMA SYSTEM receive FDA 510(k) clearance?

PRECIMED TRAUMA SYSTEM received FDA 510(k) clearance on 2000-11-09, under 510(k) number K002486.

Who is the listed applicant for PRECIMED TRAUMA SYSTEM?

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

What is the FDA product code for PRECIMED TRAUMA SYSTEM?

The FDA product code for PRECIMED TRAUMA SYSTEM is HRS.

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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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