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FDA 510(k)

LMS-LUNG/TRACK

K-Number: K070868 · 2007-05-15

ApplicantMedian Technologies
Decision Date2007-05-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LMS-LUNG/TRACK is the device name listed in this FDA 510(k) record. The listed applicant is Median Technologies. It received FDA 510(k) clearance on 2007-05-15 under 510(k) number K070868. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LMS-LUNG/TRACK?

LMS-LUNG/TRACK is a medical device that received FDA 510(k) clearance on 2007-05-15. The listed applicant is Median Technologies. The 510(k) number is K070868.

When did LMS-LUNG/TRACK receive FDA 510(k) clearance?

LMS-LUNG/TRACK received FDA 510(k) clearance on 2007-05-15, under 510(k) number K070868.

Who is the listed applicant for LMS-LUNG/TRACK?

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

What is the FDA product code for LMS-LUNG/TRACK?

The FDA product code for LMS-LUNG/TRACK is LLZ.

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Other records listing Median Technologies 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.

K251474Median LCS (internal name) / eyonis LCS (trade name) (1.0)K071241LMS-LIVER

Related Devices (Code: LLZ)

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.

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Official Source

View on FDA Database →

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

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