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FDA 510(k)

LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNEL

K-Number: K910434 · 1991-06-17

ApplicantLife Corp.
Decision Date1991-06-17
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNEL is the device name listed in this FDA 510(k) record. The listed applicant is Life Corp.. It received FDA 510(k) clearance on 1991-06-17 under 510(k) number K910434. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNEL?

LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNEL is a medical device that received FDA 510(k) clearance on 1991-06-17. The listed applicant is Life Corp.. The 510(k) number is K910434.

When did LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNEL receive FDA 510(k) clearance?

LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNEL received FDA 510(k) clearance on 1991-06-17, under 510(k) number K910434.

Who is the listed applicant for LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNEL?

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

What is the FDA product code for LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNEL?

The FDA product code for LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNEL is BTL.

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 Corp. 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.

Related Devices (Code: BTL)

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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