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FDA 510(k)

L720 EXAMINATION CHAIR

K-Number: K001261 · 2000-06-08

ApplicantLuneau Gynecologie SA
Decision Date2000-06-08
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

L720 EXAMINATION CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Luneau Gynecologie SA. It received FDA 510(k) clearance on 2000-06-08 under 510(k) number K001261. The device is classified under product code KNC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L720 EXAMINATION CHAIR?

L720 EXAMINATION CHAIR is a medical device that received FDA 510(k) clearance on 2000-06-08. The listed applicant is Luneau Gynecologie SA. The 510(k) number is K001261.

When did L720 EXAMINATION CHAIR receive FDA 510(k) clearance?

L720 EXAMINATION CHAIR received FDA 510(k) clearance on 2000-06-08, under 510(k) number K001261.

Who is the listed applicant for L720 EXAMINATION CHAIR?

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

What is the FDA product code for L720 EXAMINATION CHAIR?

The FDA product code for L720 EXAMINATION CHAIR is KNC.

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Related Devices (Code: KNC)

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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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