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FDA 510(k)

PLASMA DISCARD BAGS

K-Number: K926409 · 1993-03-02

ApplicantApheresis Technologies, Inc.
Decision Date1993-03-02
Product CodeLKN
DecisionSubstantially Equivalent

Device Summary

PLASMA DISCARD BAGS is the device name listed in this FDA 510(k) record. The listed applicant is Apheresis Technologies, Inc.. It received FDA 510(k) clearance on 1993-03-02 under 510(k) number K926409. The device is classified under product code LKN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASMA DISCARD BAGS?

PLASMA DISCARD BAGS is a medical device that received FDA 510(k) clearance on 1993-03-02. The listed applicant is Apheresis Technologies, Inc.. The 510(k) number is K926409.

When did PLASMA DISCARD BAGS receive FDA 510(k) clearance?

PLASMA DISCARD BAGS received FDA 510(k) clearance on 1993-03-02, under 510(k) number K926409.

Who is the listed applicant for PLASMA DISCARD BAGS?

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

What is the FDA product code for PLASMA DISCARD BAGS?

The FDA product code for PLASMA DISCARD BAGS is LKN.

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.

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Other records listing Apheresis Technologies, 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.

K961137ATI PLASMA PUMP (PP-04)

Related Devices (Code: LKN)

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.

K192150AMICUS Separator SystemFresenius Kabi AGK183081Spectra Optia Apheresis SystemTerumobct, Inc.K180615AMICUS Separator System, AMICUS Exchange Kit - Therapeutics, Waste Transfer Set, Blood Component Filter Set With Vented Spike and Luer AdapterFresenius Kabi USA,LlcK181049Spectra Optia Apheresis SystemTerumobct, Inc.K172590Spectra Optia Apheresis SystemTerumobct, Inc.K153601Spectra Optia Apheresis SystemTerumobct, Inc.

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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