JIMMY JOHN III
K-Number: K881720 · 1988-07-20
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Device Summary
Frequently Asked Questions
What is the JIMMY JOHN III?
JIMMY JOHN III is a medical device that received FDA 510(k) clearance on 1988-07-20. The listed applicant is Colon Therapeutics. The 510(k) number is K881720.
When did JIMMY JOHN III receive FDA 510(k) clearance?
JIMMY JOHN III received FDA 510(k) clearance on 1988-07-20, under 510(k) number K881720.
Who is the listed applicant for JIMMY JOHN III?
The FDA 510(k) record lists Colon Therapeutics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JIMMY JOHN III?
The FDA product code for JIMMY JOHN III is KPL.
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 Colon Therapeutics 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: KPL)
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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