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FDA 510(k)

IVAC VOLUMETRIC PUMP - MODEL 590

K-Number: K875332 · 1988-05-20

ApplicantY
Decision Date1988-05-20
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVAC VOLUMETRIC PUMP - MODEL 590 is the device name listed in this FDA 510(k) record. The listed applicant is Y. It received FDA 510(k) clearance on 1988-05-20 under 510(k) number K875332. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IVAC VOLUMETRIC PUMP - MODEL 590?

IVAC VOLUMETRIC PUMP - MODEL 590 is a medical device that received FDA 510(k) clearance on 1988-05-20. The listed applicant is Y. The 510(k) number is K875332.

When did IVAC VOLUMETRIC PUMP - MODEL 590 receive FDA 510(k) clearance?

IVAC VOLUMETRIC PUMP - MODEL 590 received FDA 510(k) clearance on 1988-05-20, under 510(k) number K875332.

Who is the listed applicant for IVAC VOLUMETRIC PUMP - MODEL 590?

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

What is the FDA product code for IVAC VOLUMETRIC PUMP - MODEL 590?

The FDA product code for IVAC VOLUMETRIC PUMP - MODEL 590 is FRN.

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 Y 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.

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Related Devices (Code: FRN)

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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