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FDA 510(k)

DIALYZER REPROCESSING SYSTEM DRS-4

K-Number: K821863 · 1982-10-18

Decision Date1982-10-18
Product CodeLIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIALYZER REPROCESSING SYSTEM DRS-4 is the device name listed in this FDA 510(k) record. The listed applicant is Seratronics, Inc.. It received FDA 510(k) clearance on 1982-10-18 under 510(k) number K821863. 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 DIALYZER REPROCESSING SYSTEM DRS-4?

DIALYZER REPROCESSING SYSTEM DRS-4 is a medical device that received FDA 510(k) clearance on 1982-10-18. The listed applicant is Seratronics, Inc.. The 510(k) number is K821863.

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

DIALYZER REPROCESSING SYSTEM DRS-4 received FDA 510(k) clearance on 1982-10-18, under 510(k) number K821863.

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

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 DIALYZER REPROCESSING SYSTEM DRS-4?

The FDA product code for DIALYZER REPROCESSING SYSTEM DRS-4 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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