MODIFIED JIMMY JOHN III
K-Number: K870127 · 1987-03-17
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Device Summary
Frequently Asked Questions
What is the MODIFIED JIMMY JOHN III?
MODIFIED JIMMY JOHN III is a medical device that received FDA 510(k) clearance on 1987-03-17. The listed applicant is Colon Therapeutics. The 510(k) number is K870127.
When did MODIFIED JIMMY JOHN III receive FDA 510(k) clearance?
MODIFIED JIMMY JOHN III received FDA 510(k) clearance on 1987-03-17, under 510(k) number K870127.
Who is the listed applicant for MODIFIED 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 MODIFIED JIMMY JOHN III?
The FDA product code for MODIFIED 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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