Nagashima SN Automatic Treatment Chair

FDA 510(k) K822013 · Kelleher Corp.

Substantially Equivalent

510(k) numberK822013

Submission

Device name
Nagashima SN Automatic Treatment Chair
Applicant
Kelleher Corp.
Mchenry, IL, US
Received
July 8, 1982
Decision date
July 28, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GBB – Chair, Surgical, Ac-Powered
Device class
Class I (low risk)
Regulation
21 CFR 878.4960
Specialty
General, Plastic Surgery

Other 510(k)s with product code GBB

510(k)DeviceApplicantDecision
K964102Tenet Tibial Fracture SupportGBB · Traditional Tenet Medical Engineering12/05/1996SE
K893598Hydraulic Foot Operated StoolGBB · Traditional Arthro-Medic, Inc.10/10/1989SE
K831385Lithotomy Chair #415GBB · Traditional Midmark Corp.06/02/1983SE
K831325NutromatGBB · Traditional Medlog GmbH Marketing Services06/02/1983SE
K822264Nagashima SN Operator's ChairGBB · Traditional Kelleher Corp.10/13/1982SE
K822251Examination & Treatment ChairsGBB · Traditional Kelleher Corp.08/27/1982SE
K820636Storz #6500 Power Examination ChairGBB · Traditional Storz Instrument Co.03/26/1982SE

More from Storz Instrument Co.

510(k)DeviceDecision
K822618Emergency Tracheostomy Instrument SetLJW · Traditional 01/28/1983SE
K822268Nagashima Ns-Iii ElectronystagmographGWN · Traditional 01/28/1983SE
K823083Electrosurgical UnitGEI · Traditional 12/07/1982SE
K823111Nystymograph AccessGNN · Traditional 11/22/1982SE
K822252ENT Treatment UnitsETF · Traditional 11/22/1982SE
K822272Head Mirrors W/Head Lamps & Head BandsHPQ · Traditional 11/10/1982SE
K822017Tympanostomy Tubes & Various TypesETD · Traditional 10/27/1982SE
K822257Various Types of Light Source HandlesEOQ · Traditional 10/26/1982SE
K822259Laryngeal SpatulasEQH · Traditional 10/22/1982SE
K822004Face ShieldsKNT · Traditional 10/20/1982SE

Questions and answers

When was Nagashima SN Automatic Treatment Chair cleared by the FDA?

Nagashima SN Automatic Treatment Chair (K822013) received a 510(k) decision of Substantially Equivalent on July 28, 1982, 20 days after the submission was received.

What is the product code of K822013?

The FDA product code is GBB – Chair, Surgical, Ac-Powered, a Class I (low risk) device regulated under 21 CFR 878.4960.