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FDA 510(k)

IVFLO-HP & IVFIL-HP FILTER

K-Number: K831350 · 1983-08-12

ApplicantTri-Med, Inc.
Decision Date1983-08-12
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVFLO-HP & IVFIL-HP FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Med, Inc.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K831350. The device is classified under product code FPB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IVFLO-HP & IVFIL-HP FILTER?

IVFLO-HP & IVFIL-HP FILTER is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Tri-Med, Inc.. The 510(k) number is K831350.

When did IVFLO-HP & IVFIL-HP FILTER receive FDA 510(k) clearance?

IVFLO-HP & IVFIL-HP FILTER received FDA 510(k) clearance on 1983-08-12, under 510(k) number K831350.

Who is the listed applicant for IVFLO-HP & IVFIL-HP FILTER?

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

What is the FDA product code for IVFLO-HP & IVFIL-HP FILTER?

The FDA product code for IVFLO-HP & IVFIL-HP FILTER is FPB.

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 Tri-Med, 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 29 devices →

Related Devices (Code: FPB)

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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