Power Examination Table

FDA 510(k) K882010 · Enochs Mfg., Inc.

Substantially Equivalent

510(k) numberK882010

Submission

Device name
Power Examination Table
Applicant
Enochs Mfg., Inc.
Indianapolis, IN, US
Received
May 13, 1988
Decision date
July 13, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LGX – Table, Examination, Medical, Powered
Device class
Class I (low risk)
Regulation
21 CFR 878.4960
Specialty
General, Plastic Surgery

Other 510(k)s with product code LGX

510(k)DeviceApplicantDecision
K945163EchocardiographyLGX · Traditional Tri W-G, Inc.02/17/1995SE
K894144Power Examination Table Model # 405LGX · Traditional Midmark Corp.08/28/1989SE
K894134Power Examination Table Model # 411LGX · Traditional Midmark Corp.08/28/1989SE
K883680Medalist Examination TableLGX · Traditional Hamilton Industries, Inc.10/04/1988SE
K864072Adec 1005-C ChairLGX · Traditional Cherne Industries, Inc.11/07/1986SE
K860519Reliance Model 200 Podiatry ChairLGX · Traditional F. & F. Koenigkramer02/19/1986SE
K845023Storz Plastic Surgery & Examination Lounge 7000LGX · Traditional Storz Instrument Co.01/28/1985SE
K830294Medical Exam TableLGX · Traditional Coe Laboratories, Inc.01/11/1984SE
K832768S & W SW52E W/Power Back LiftLGX · Traditional S & W Enterprises, Inc.09/20/1983SE
K820823Multiple, Model #17LGX · Traditional Midmark Corp.04/21/1982SE

Questions and answers

When was Power Examination Table cleared by the FDA?

Power Examination Table (K882010) received a 510(k) decision of Substantially Equivalent on July 13, 1988, 61 days after the submission was received.

What is the product code of K882010?

The FDA product code is LGX – Table, Examination, Medical, Powered, a Class I (low risk) device regulated under 21 CFR 878.4960.