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)

EASYFIL

K-Number: K790448 · 1979-04-11

Decision Date1979-04-11
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EASYFIL is the device name listed in this FDA 510(k) record. The listed applicant is General Refineries, Inc.. It received FDA 510(k) clearance on 1979-04-11 under 510(k) number K790448. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYFIL?

EASYFIL is a medical device that received FDA 510(k) clearance on 1979-04-11. The listed applicant is General Refineries, Inc.. The 510(k) number is K790448.

When did EASYFIL receive FDA 510(k) clearance?

EASYFIL received FDA 510(k) clearance on 1979-04-11, under 510(k) number K790448.

Who is the listed applicant for EASYFIL?

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

What is the FDA product code for EASYFIL?

The FDA product code for EASYFIL is EJJ.

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.

Related Devices (Code: EJJ)

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.

↑