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)

E-Z JECTOR

K-Number: K830042 · 1983-01-26

Decision Date1983-01-26
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

E-Z JECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Innovators, Inc.. It received FDA 510(k) clearance on 1983-01-26 under 510(k) number K830042. The device is classified under product code EJI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-Z JECTOR?

E-Z JECTOR is a medical device that received FDA 510(k) clearance on 1983-01-26. The listed applicant is Innovators, Inc.. The 510(k) number is K830042.

When did E-Z JECTOR receive FDA 510(k) clearance?

E-Z JECTOR received FDA 510(k) clearance on 1983-01-26, under 510(k) number K830042.

Who is the listed applicant for E-Z JECTOR?

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

What is the FDA product code for E-Z JECTOR?

The FDA product code for E-Z JECTOR is EJI.

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 Innovators, 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.

Related Devices (Code: EJI)

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.

↑