Rt-Hood

FDA 510(k) K790860 · Plastics Supplies & Products

Substantially Equivalent

510(k) numberK790860

Submission

Device name
Rt-Hood
Applicant
Plastics Supplies & Products
Mchenry, IL, US
Received
May 7, 1979
Decision date
May 29, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FOG – Hood, Oxygen, Infant
Device class
Class I (low risk)
Regulation
21 CFR 868.5700
Specialty
Anesthesiology

Other 510(k)s with product code FOG

510(k)DeviceApplicantDecision
K973128Olympus NA-10J-1 Aspiration NeedleFOG · Traditional Olympus America, Inc.11/18/1997SE
K962182Burlew Infant HoodFOG · Traditional Promedic, Inc.07/15/1996SE
K955482Swift Infant Oxygen Hood-Reusable (Modification)FOG · Traditional Advantage Medical Services, Inc.01/30/1996SE
K830781Endo-GuardFOG · Traditional Jayco Pharmaceuticals03/31/1983SE
K792144Disposa-HoodFOG · Traditional Utah Medical Products, Inc.12/05/1979SE
K791861Oxygen HoodsFOG · Traditional Ann Arbor Plastics, Inc.10/04/1979SE
K780220Hood, Infant OxygenFOG · Traditional Shiley, Inc.04/10/1978SE
K770754Duodenoscope, Molel TX-6FOG · Traditional American Cystocope Makers, Inc.04/28/1977SE

Questions and answers

When was Rt-Hood cleared by the FDA?

Rt-Hood (K790860) received a 510(k) decision of Substantially Equivalent on May 29, 1979, 22 days after the submission was received.

What is the product code of K790860?

The FDA product code is FOG – Hood, Oxygen, Infant, a Class I (low risk) device regulated under 21 CFR 868.5700.