JEL-0-75
K-Number: K923716 · 1993-03-05
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Device Summary
Frequently Asked Questions
What is the JEL-0-75?
JEL-0-75 is a medical device that received FDA 510(k) clearance on 1993-03-05. The listed applicant is J.F. Jelenko & Co., Inc.. The 510(k) number is K923716.
When did JEL-0-75 receive FDA 510(k) clearance?
JEL-0-75 received FDA 510(k) clearance on 1993-03-05, under 510(k) number K923716.
Who is the listed applicant for JEL-0-75?
The FDA 510(k) record lists J.F. Jelenko & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JEL-0-75?
The FDA product code for JEL-0-75 is EJT.
Other records listing J.F. Jelenko & Co., 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: EJT)
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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