LSP Demand Inhalator Valve Model SPOO68 W/Mask

FDA 510(k) K884543 · Sechrist Industries, Inc.

Substantially Equivalent

510(k) numberK884543

Submission

Device name
LSP Demand Inhalator Valve Model SPOO68 W/Mask
Applicant
Sechrist Industries, Inc.
Anaheim, CA, US
Received
October 31, 1988
Decision date
December 13, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CBP – Valve, Non-Rebreathing
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5870
Specialty
Anesthesiology
Life-sustaining
Yes

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More from Intersurgical Incorporated

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K140559Sechrist Monoplace Hyperbaric Oxygen ChamberCBF · Special 05/30/2014SE
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K052713Model 3300E/ER Monoplace Hyperbaric Oxygen ChamberCBF · Special 10/28/2005SE
K023745Sechrist Air/Oxygen Mixer, Model 3500 Cp-GDTX · Traditional 01/17/2003SE
K993167Millennium Infant VentilatorCBK · Special 11/10/1999ST
K992503Sechrist Air-Oxygen Mixer, 3500/3500HL SeriesBZR · Special 08/10/1999SE
K950386Model 3200P/3200PR Hyperbaric ChamberCBF · Traditional 06/13/1995SE
K934164Model 2500E/2500ER Hyperbaric ChamberCBF · Traditional 06/13/1995SE
K930713The Infant Flow SystemCAI · Traditional 09/16/1993SE
K914607Sehrist Volume Ventilator, Model 2200BCBK · Traditional 11/02/1992SE

Questions and answers

When was LSP Demand Inhalator Valve Model SPOO68 W/Mask cleared by the FDA?

LSP Demand Inhalator Valve Model SPOO68 W/Mask (K884543) received a 510(k) decision of Substantially Equivalent on December 13, 1988, 43 days after the submission was received.

What is the product code of K884543?

The FDA product code is CBP – Valve, Non-Rebreathing, a Class II (moderate risk) device regulated under 21 CFR 868.5870.