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FDA 510(k)

PROBLOC, HN SERIES AND PROLONG, PL SERIES

K-Number: K050499 · 2005-05-17

ApplicantLife-Tech, Inc.
Decision Date2005-05-17
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PROBLOC, HN SERIES AND PROLONG, PL SERIES 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 2005-05-17 under 510(k) number K050499. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROBLOC, HN SERIES AND PROLONG, PL SERIES?

PROBLOC, HN SERIES AND PROLONG, PL SERIES is a medical device that received FDA 510(k) clearance on 2005-05-17. The listed applicant is Life-Tech, Inc.. The 510(k) number is K050499.

When did PROBLOC, HN SERIES AND PROLONG, PL SERIES receive FDA 510(k) clearance?

PROBLOC, HN SERIES AND PROLONG, PL SERIES received FDA 510(k) clearance on 2005-05-17, under 510(k) number K050499.

Who is the listed applicant for PROBLOC, HN SERIES AND PROLONG, PL SERIES?

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 PROBLOC, HN SERIES AND PROLONG, PL SERIES?

The FDA product code for PROBLOC, HN SERIES AND PROLONG, PL SERIES is BSP.

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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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