Converta-Litter

FDA 510(k) K874060 · Camtec

Substantially Equivalent

510(k) numberK874060

Submission

Device name
Converta-Litter
Applicant
Camtec
Cambridge, MD, US
Received
October 5, 1987
Decision date
December 10, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
INN – Chair, Adjustable, Mechanical
Device class
Class I (low risk)
Regulation
21 CFR 890.3100
Specialty
Physical Medicine

Other 510(k)s with product code INN

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K945650SpiffyINN · Traditional Thames Valley Children'S Centre12/19/1994SE
K942397Theradapt Highchair/Stroller InsertINN · Traditional Theradapt Products, Inc.06/22/1994SE
K930520Theradapt(R) Adjustable Classroom ChairINN · Traditional Theradapt Products, Inc.03/24/1993SE
K923753Able Generation Therapy Tilt BenchINN · Traditional The Able Generation, Inc.01/29/1993SE
K923752Able Generation Play ChairINN · Traditional The Able Generation, Inc.01/29/1993SE
K923750Able Generation Booster ChairINN · Traditional The Able Generation, Inc.01/29/1993SE
K923095Kaye Model Kiao Pelvic/Thigh StabilizerINN · Traditional Kaye Products, Inc.07/21/1992SE
K922061Chair, Adjustable, MechanicalINN · Traditional Kaye Products, Inc.05/26/1992SE
K921272Activity ChairINN · Traditional Rifton Equipment For the Handicapped04/07/1992SE
K904069Broda Nursing Care ChairINN · Traditional Broda Ent., Inc.09/17/1990SE

More from Broda Ent., Inc.

510(k)DeviceDecision
K872729Infusion StandFOX · Traditional 07/23/1987SE

Questions and answers

When was Converta-Litter cleared by the FDA?

Converta-Litter (K874060) received a 510(k) decision of Substantially Equivalent on December 10, 1987, 66 days after the submission was received.

What is the product code of K874060?

The FDA product code is INN – Chair, Adjustable, Mechanical, a Class I (low risk) device regulated under 21 CFR 890.3100.