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FDA 510(k)

RENALIN REUSE CART

K-Number: K941867 · 1996-01-22

ApplicantRenal Scientific Service, Inc.
Decision Date1996-01-22
Product CodeLIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RENALIN REUSE CART is the device name listed in this FDA 510(k) record. The listed applicant is Renal Scientific Service, Inc.. It received FDA 510(k) clearance on 1996-01-22 under 510(k) number K941867. The device is classified under product code LIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RENALIN REUSE CART?

RENALIN REUSE CART is a medical device that received FDA 510(k) clearance on 1996-01-22. The listed applicant is Renal Scientific Service, Inc.. The 510(k) number is K941867.

When did RENALIN REUSE CART receive FDA 510(k) clearance?

RENALIN REUSE CART received FDA 510(k) clearance on 1996-01-22, under 510(k) number K941867.

Who is the listed applicant for RENALIN REUSE CART?

The FDA 510(k) record lists Renal Scientific Service, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RENALIN REUSE CART?

The FDA product code for RENALIN REUSE CART is LIF.

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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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