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FDA 510(k)

PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS

K-Number: K072050 · 2007-10-18

ApplicantLife-Tech, Inc.
Decision Date2007-10-18
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech, Inc.. It received FDA 510(k) clearance on 2007-10-18 under 510(k) number K072050. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS?

PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS is a medical device that received FDA 510(k) clearance on 2007-10-18. The listed applicant is Life-Tech, Inc.. The 510(k) number is K072050.

When did PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS receive FDA 510(k) clearance?

PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS received FDA 510(k) clearance on 2007-10-18, under 510(k) number K072050.

Who is the listed applicant for PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS?

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

What is the FDA product code for PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS?

The FDA product code for PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS is BSO.

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Other records listing Life-Tech, Inc. as applicant

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Related Devices (Code: BSO)

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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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