JEL-71 PDF
K-Number: K971292 · 1997-05-20
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Device Summary
Frequently Asked Questions
What is the JEL-71 PDF?
JEL-71 PDF is a medical device that received FDA 510(k) clearance on 1997-05-20. The listed applicant is J.F. Jelenko & Co., Inc.. The 510(k) number is K971292.
When did JEL-71 PDF receive FDA 510(k) clearance?
JEL-71 PDF received FDA 510(k) clearance on 1997-05-20, under 510(k) number K971292.
Who is the listed applicant for JEL-71 PDF?
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-71 PDF?
The FDA product code for JEL-71 PDF 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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