JIMMY JOHN III, RECTAL NOZZLE (MODIFICATION)— 510(k) K860943

Name: FDA 510(k) clearance K860943
Creator: U.S. Food and Drug Administration
Published: 1986-05-15

Substantially Equivalent

Colon Therapeutics

FDA 510(k) clearance K860943 for JIMMY JOHN III, RECTAL NOZZLE (MODIFICATION), Substantially Equivalent on 1986-05-15. Applicant: Colon Therapeutics. Device class: 2.

Clearance details

Applicant: Colon Therapeutics
Product code: Code KPL
Device class: Class 2
Regulation: 21 CFR 876.5220
Advisory panel: Gastroenterology, Urology
Date received: 1986-03-12
Decision date: 1986-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Port Arthur, TX, US

Download summary PDF View on FDA.gov ↗

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K150381 — AQUA CLEANSE2015-09-11
K131852 — HC-1 AND HC-1 CLASSIC2014-04-17

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K973256 — JIMMY JOHN III RECTAL NOZZLE1997-09-29
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K881720 — JIMMY JOHN III1988-07-20
K873948 — MODIFIED RECTAL NOZZLE1987-10-14
K870127 — MODIFIED JIMMY JOHN III1987-03-17

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