ALLROUND 4
K-Number: K944889 · 1994-11-17
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Device Summary
Frequently Asked Questions
What is the ALLROUND 4?
ALLROUND 4 is a medical device that received FDA 510(k) clearance on 1994-11-17. The listed applicant is J.F. Jelenko & Co., Inc.. The 510(k) number is K944889.
When did ALLROUND 4 receive FDA 510(k) clearance?
ALLROUND 4 received FDA 510(k) clearance on 1994-11-17, under 510(k) number K944889.
Who is the listed applicant for ALLROUND 4?
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 ALLROUND 4?
The FDA product code for ALLROUND 4 is EJT.
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 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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