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FDA 510(k)

LSP DISPOSABLE BAG RESUSCITATOR, MODEL 470

K-Number: K874418 · 1988-01-22

Decision Date1988-01-22
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LSP DISPOSABLE BAG RESUSCITATOR, MODEL 470 is the device name listed in this FDA 510(k) record. The listed applicant is Life Support Products, Inc.. It received FDA 510(k) clearance on 1988-01-22 under 510(k) number K874418. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LSP DISPOSABLE BAG RESUSCITATOR, MODEL 470?

LSP DISPOSABLE BAG RESUSCITATOR, MODEL 470 is a medical device that received FDA 510(k) clearance on 1988-01-22. The listed applicant is Life Support Products, Inc.. The 510(k) number is K874418.

When did LSP DISPOSABLE BAG RESUSCITATOR, MODEL 470 receive FDA 510(k) clearance?

LSP DISPOSABLE BAG RESUSCITATOR, MODEL 470 received FDA 510(k) clearance on 1988-01-22, under 510(k) number K874418.

Who is the listed applicant for LSP DISPOSABLE BAG RESUSCITATOR, MODEL 470?

The FDA 510(k) record lists Life Support Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LSP DISPOSABLE BAG RESUSCITATOR, MODEL 470?

The FDA product code for LSP DISPOSABLE BAG RESUSCITATOR, MODEL 470 is BTM.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Life Support Products, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 20 devices →

Related Devices (Code: BTM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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