LSP Disposable Bag Resuscitator, Model 470

FDA 510(k) K874418 · Life Support Products, Inc.

Substantially Equivalent

510(k) numberK874418

Submission

Device name
LSP Disposable Bag Resuscitator, Model 470
Applicant
Life Support Products, Inc.
Irvine, CA, US
Received
October 28, 1987
Decision date
January 22, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BTM – Ventilator, Emergency, Manual (Resuscitator)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5915
Specialty
Anesthesiology
Life-sustaining
Yes

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K212905Sotair DeviceBTM · Traditional Safe Bvm Corporation08/18/2022SE
K210288Disposable Manual ResuscitatorBTM · Traditional Xiamen Compower Medical Tech. Co., Ltd.08/26/2021SE
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K170663Foremount Disposable PVC Resuscitator, Foremount Disposable PEEP Valve, Foremount…BTM · Traditional Foremount Enterprise Co., Ltd.05/11/2018SE
K152931Ambu SPUR II Adult Resuscitator, Ambu SPUR II Pediatric Resuscitator, Ambu SPUR II…BTM · Abbreviated Ambu A/S08/29/2016SE
K132172Neonatalie ResuscitatorBTM · Abbreviated Laerdal Medical A/S01/15/2015SE
K112852Babi Plus Neonatal Resuscitation BagBTM · Traditional A Plus Medical01/13/2012SE

More from A Plus Medical

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K940934Life VacBTA · Traditional 05/03/1994SE
K936187Lspi Pressure RegulatorCAN · Traditional 01/27/1994SE
K932200Lspi Automatic VentilatorBTL · Traditional 11/24/1993SE
K932199Lspi Automatic Ventilator, Model AV3000BTL · Traditional 11/24/1993SE
K922819Infant Disposable Bag Mask ResuscitatorBTM · Traditional 11/24/1993SE
K922691LSP (Model 554) Bag Mask ResuscitatorBTM · Traditional 11/24/1993SE
K921553Lspi Infant Bag MaskBTM · Traditional 10/19/1992SE
K924217Lspi Disposable Bag Mask Resuscitator/ModifiedBTM · Traditional 09/17/1992SE

Questions and answers

When was LSP Disposable Bag Resuscitator, Model 470 cleared by the FDA?

LSP Disposable Bag Resuscitator, Model 470 (K874418) received a 510(k) decision of Substantially Equivalent on January 22, 1988, 86 days after the submission was received.

What is the product code of K874418?

The FDA product code is BTM – Ventilator, Emergency, Manual (Resuscitator), a Class II (moderate risk) device regulated under 21 CFR 868.5915.