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FDA 510(k)

SAMSON'S NEWBORN LUNG INFLATOR 340-1000

K-Number: K842487 · 1984-07-06

Decision Date1984-07-06
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SAMSON'S NEWBORN LUNG INFLATOR 340-1000 is the device name listed in this FDA 510(k) record. The listed applicant is J. H. Emerson Co.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K842487. 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 SAMSON'S NEWBORN LUNG INFLATOR 340-1000?

SAMSON'S NEWBORN LUNG INFLATOR 340-1000 is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is J. H. Emerson Co.. The 510(k) number is K842487.

When did SAMSON'S NEWBORN LUNG INFLATOR 340-1000 receive FDA 510(k) clearance?

SAMSON'S NEWBORN LUNG INFLATOR 340-1000 received FDA 510(k) clearance on 1984-07-06, under 510(k) number K842487.

Who is the listed applicant for SAMSON'S NEWBORN LUNG INFLATOR 340-1000?

The FDA 510(k) record lists J. H. Emerson Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAMSON'S NEWBORN LUNG INFLATOR 340-1000?

The FDA product code for SAMSON'S NEWBORN LUNG INFLATOR 340-1000 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 J. H. Emerson Co. 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 25 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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