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FDA 510(k)

DRS-4 DIALYZER REPROCESSING SYSTEM

K-Number: K860674 · 1986-04-07

Decision Date1986-04-07
Product CodeLIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DRS-4 DIALYZER REPROCESSING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Seratronics, Inc.. It received FDA 510(k) clearance on 1986-04-07 under 510(k) number K860674. 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 DRS-4 DIALYZER REPROCESSING SYSTEM?

DRS-4 DIALYZER REPROCESSING SYSTEM is a medical device that received FDA 510(k) clearance on 1986-04-07. The listed applicant is Seratronics, Inc.. The 510(k) number is K860674.

When did DRS-4 DIALYZER REPROCESSING SYSTEM receive FDA 510(k) clearance?

DRS-4 DIALYZER REPROCESSING SYSTEM received FDA 510(k) clearance on 1986-04-07, under 510(k) number K860674.

Who is the listed applicant for DRS-4 DIALYZER REPROCESSING SYSTEM?

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

What is the FDA product code for DRS-4 DIALYZER REPROCESSING SYSTEM?

The FDA product code for DRS-4 DIALYZER REPROCESSING SYSTEM is LIF.

Related Clinical Trials

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.

Other records listing Seratronics, Inc. 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.

View all 21 devices →

Related Devices (Code: LIF)

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.

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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