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)

EZY-RAMP

K-Number: K841994 · 1984-05-23

ApplicantEzy-Ramp Co.
Decision Date1984-05-23
Product Code
DecisionSubstantially Equivalent

Device Summary

EZY-RAMP is the device name listed in this FDA 510(k) record. The listed applicant is Ezy-Ramp Co.. It received FDA 510(k) clearance on 1984-05-23 under 510(k) number K841994. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZY-RAMP?

EZY-RAMP is a medical device that received FDA 510(k) clearance on 1984-05-23. The listed applicant is Ezy-Ramp Co.. The 510(k) number is K841994.

When did EZY-RAMP receive FDA 510(k) clearance?

EZY-RAMP received FDA 510(k) clearance on 1984-05-23, under 510(k) number K841994.

Who is the listed applicant for EZY-RAMP?

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

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.

↑