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FDA 510(k)

D-3260 SORBENT CARTRIDGE

K-Number: K812869 · 1981-12-08

ApplicantOrganon Teknika Corp.
Decision Date1981-12-08
Product CodeFKT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

D-3260 SORBENT CARTRIDGE is the device name listed in this FDA 510(k) record. The listed applicant is Organon Teknika Corp.. It received FDA 510(k) clearance on 1981-12-08 under 510(k) number K812869. The device is classified under product code FKT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the D-3260 SORBENT CARTRIDGE?

D-3260 SORBENT CARTRIDGE is a medical device that received FDA 510(k) clearance on 1981-12-08. The listed applicant is Organon Teknika Corp.. The 510(k) number is K812869.

When did D-3260 SORBENT CARTRIDGE receive FDA 510(k) clearance?

D-3260 SORBENT CARTRIDGE received FDA 510(k) clearance on 1981-12-08, under 510(k) number K812869.

Who is the listed applicant for D-3260 SORBENT CARTRIDGE?

The FDA 510(k) record lists Organon Teknika Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for D-3260 SORBENT CARTRIDGE?

The FDA product code for D-3260 SORBENT CARTRIDGE is FKT.

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Other records listing Organon Teknika Corp. as applicant

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Related Devices (Code: FKT)

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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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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