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FDA 510(k)

LIFERX

K-Number: K001596 · 2000-07-06

ApplicantBowdengs Technologies, LLC
Decision Date2000-07-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LIFERX is the device name listed in this FDA 510(k) record. The listed applicant is Bowdengs Technologies, LLC. It received FDA 510(k) clearance on 2000-07-06 under 510(k) number K001596. 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 LIFERX?

LIFERX is a medical device that received FDA 510(k) clearance on 2000-07-06. The listed applicant is Bowdengs Technologies, LLC. The 510(k) number is K001596.

When did LIFERX receive FDA 510(k) clearance?

LIFERX received FDA 510(k) clearance on 2000-07-06, under 510(k) number K001596.

Who is the listed applicant for LIFERX?

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

What is the FDA product code for LIFERX?

The FDA product code for LIFERX is LLZ.

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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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