MED-E-JET INJECTOR
K-Number: K913018 · 1991-09-16
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Device Summary
Frequently Asked Questions
What is the MED-E-JET INJECTOR?
MED-E-JET INJECTOR is a medical device that received FDA 510(k) clearance on 1991-09-16. The listed applicant is Med-E-Jet D. The 510(k) number is K913018.
When did MED-E-JET INJECTOR receive FDA 510(k) clearance?
MED-E-JET INJECTOR received FDA 510(k) clearance on 1991-09-16, under 510(k) number K913018.
Who is the listed applicant for MED-E-JET INJECTOR?
The FDA 510(k) record lists Med-E-Jet D as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MED-E-JET INJECTOR?
The FDA product code for MED-E-JET INJECTOR is KZE.
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: KZE)
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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