Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

INFUSION PUMP MODEL 470

K-Number: K872515 · 1987-12-16

ApplicantAvi, Inc.
Decision Date1987-12-16
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUSION PUMP MODEL 470 is the device name listed in this FDA 510(k) record. The listed applicant is Avi, Inc.. It received FDA 510(k) clearance on 1987-12-16 under 510(k) number K872515. 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 INFUSION PUMP MODEL 470?

INFUSION PUMP MODEL 470 is a medical device that received FDA 510(k) clearance on 1987-12-16. The listed applicant is Avi, Inc.. The 510(k) number is K872515.

When did INFUSION PUMP MODEL 470 receive FDA 510(k) clearance?

INFUSION PUMP MODEL 470 received FDA 510(k) clearance on 1987-12-16, under 510(k) number K872515.

Who is the listed applicant for INFUSION PUMP MODEL 470?

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

What is the FDA product code for INFUSION PUMP MODEL 470?

The FDA product code for INFUSION PUMP MODEL 470 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 Avi, 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 13 devices →

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.

↑