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FDA 510(k)

LIFEPORT ATTACHABLE SYSTEM W/INDUCER KIT LPS 5555

K-Number: K915273 · 1993-07-07

Decision Date1993-07-07
Product CodeLJT
Advisory CommitteeHO
DecisionUnknown

Device Summary

LIFEPORT ATTACHABLE SYSTEM W/INDUCER KIT LPS 5555 is the device name listed in this FDA 510(k) record. The listed applicant is Strato Medical Corp.. It received FDA 510(k) clearance on 1993-07-07 under 510(k) number K915273. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the LIFEPORT ATTACHABLE SYSTEM W/INDUCER KIT LPS 5555?

LIFEPORT ATTACHABLE SYSTEM W/INDUCER KIT LPS 5555 is a medical device that received FDA 510(k) clearance on 1993-07-07. The listed applicant is Strato Medical Corp.. The 510(k) number is K915273.

When did LIFEPORT ATTACHABLE SYSTEM W/INDUCER KIT LPS 5555 receive FDA 510(k) clearance?

LIFEPORT ATTACHABLE SYSTEM W/INDUCER KIT LPS 5555 received FDA 510(k) clearance on 1993-07-07, under 510(k) number K915273.

Who is the listed applicant for LIFEPORT ATTACHABLE SYSTEM W/INDUCER KIT LPS 5555?

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

What is the FDA product code for LIFEPORT ATTACHABLE SYSTEM W/INDUCER KIT LPS 5555?

The FDA product code for LIFEPORT ATTACHABLE SYSTEM W/INDUCER KIT LPS 5555 is LJT.

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 Strato Medical 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.

View all 45 devices →

Related Devices (Code: LJT)

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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