L720 Examination Chair

FDA 510(k) K001261 · Luneau Gynecologie SA

Substantially Equivalent

510(k) numberK001261

Submission

Device name
L720 Examination Chair
Applicant
Luneau Gynecologie SA
Chartres Cedex, FR
Received
April 19, 2000
Decision date
June 8, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KNC – Table, Obstetric (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 884.4900
Specialty
Obstetrics/Gynecology

Other 510(k)s with product code KNC

510(k)DeviceApplicantDecision
K932035Non-Linting Delivery BlanketKNC · Traditional Amsco Sterile Recoveries, Inc.05/26/1994SE
K924420Medical Disposable BeddingKNC · Traditional Hill-Rom, Inc.12/10/1993SE
K914544BD6000 the Optima & BD5000 Birthing BedKNC · Traditional Lic Care, Inc.11/24/1993SE
K915779Affinity Bed Model 3600 SeriesKNC · Traditional Hill-Rom, Inc.02/24/1993SE
K903973Gardosi Birthing CushionKNC · Traditional Graphic Controls Corp.09/27/1990SE
K884868Obstetrical Safety SystemKNC · Traditional Buckman Co., Inc.03/01/1989SE
K870745Stryker Model 977 Birthing BedKNC · Traditional Stryker Corp.02/27/1987SE
K864194Palmer Obstetric BraceKNC · Traditional Ad-Tech Medical Instrument Corp01/14/1987SE
K862931Merivaara Obstetric Chair/Bed-Model 358KNC · Traditional Global Medical Prods, Inc.08/07/1986SE
K861030Labor-Delivery Stretch/BedKNC · Traditional Adel Medical , Ltd.04/23/1986SE

Questions and answers

When was L720 Examination Chair cleared by the FDA?

L720 Examination Chair (K001261) received a 510(k) decision of Substantially Equivalent on June 8, 2000, 50 days after the submission was received.

What is the product code of K001261?

The FDA product code is KNC – Table, Obstetric (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.4900.