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FDA 510(k)

B2C, ESPACE REVISION CUP SYSTEM

K-Number: K990523 · 1999-04-30

ApplicantTurnkey Intergration USA, Inc.
Decision Date1999-04-30
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

B2C, ESPACE REVISION CUP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Turnkey Intergration USA, Inc.. It received FDA 510(k) clearance on 1999-04-30 under 510(k) number K990523. 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 B2C, ESPACE REVISION CUP SYSTEM?

B2C, ESPACE REVISION CUP SYSTEM is a medical device that received FDA 510(k) clearance on 1999-04-30. The listed applicant is Turnkey Intergration USA, Inc.. The 510(k) number is K990523.

When did B2C, ESPACE REVISION CUP SYSTEM receive FDA 510(k) clearance?

B2C, ESPACE REVISION CUP SYSTEM received FDA 510(k) clearance on 1999-04-30, under 510(k) number K990523.

Who is the listed applicant for B2C, ESPACE REVISION CUP SYSTEM?

The FDA 510(k) record lists Turnkey Intergration USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for B2C, ESPACE REVISION CUP SYSTEM?

The FDA product code for B2C, ESPACE REVISION CUP SYSTEM is LPH.

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Related Devices (Code: LPH)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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