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FDA 510(k)

CARDIFF ALDASORBER SYSTEM

K-Number: K811703 · 1981-06-16

ApplicantWilliam Harvey Life Products Corp.
Decision Date1981-06-16
Product Code
DecisionUnknown

Device Summary

CARDIFF ALDASORBER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is William Harvey Life Products Corp.. It received FDA 510(k) clearance on 1981-06-16 under 510(k) number K811703. FDA Decision: Unknown.

Frequently Asked Questions

What is the CARDIFF ALDASORBER SYSTEM?

CARDIFF ALDASORBER SYSTEM is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is William Harvey Life Products Corp.. The 510(k) number is K811703.

When did CARDIFF ALDASORBER SYSTEM receive FDA 510(k) clearance?

CARDIFF ALDASORBER SYSTEM received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811703.

Who is the listed applicant for CARDIFF ALDASORBER SYSTEM?

The FDA 510(k) record lists William Harvey Life Products Corp. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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Other records listing William Harvey Life Products Corp. 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.

K810065SCOTT CM42 PASTEURIZERK770720TUBING PACK, EXTRACORPOREAL, H-3000

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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