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FDA 510(k)

ESOP CO-CR FEMORAL HEADS

K-Number: K021109 · 2002-06-12

Decision Date2002-06-12
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ESOP CO-CR FEMORAL HEADS is the device name listed in this FDA 510(k) record. The listed applicant is Fournitures Hospitalieres. It received FDA 510(k) clearance on 2002-06-12 under 510(k) number K021109. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESOP CO-CR FEMORAL HEADS?

ESOP CO-CR FEMORAL HEADS is a medical device that received FDA 510(k) clearance on 2002-06-12. The listed applicant is Fournitures Hospitalieres. The 510(k) number is K021109.

When did ESOP CO-CR FEMORAL HEADS receive FDA 510(k) clearance?

ESOP CO-CR FEMORAL HEADS received FDA 510(k) clearance on 2002-06-12, under 510(k) number K021109.

Who is the listed applicant for ESOP CO-CR FEMORAL HEADS?

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

What is the FDA product code for ESOP CO-CR FEMORAL HEADS?

The FDA product code for ESOP CO-CR FEMORAL HEADS is LPH.

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 Fournitures Hospitalieres 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.

Related Devices (Code: LPH)

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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