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FDA 510(k)

JIMMY JOHN III RECTAL NOZZLE

K-Number: K973256 · 1997-09-29

ApplicantColon Therapeutics
Decision Date1997-09-29
Product CodeKPL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

JIMMY JOHN III RECTAL NOZZLE is the device name listed in this FDA 510(k) record. The listed applicant is Colon Therapeutics. It received FDA 510(k) clearance on 1997-09-29 under 510(k) number K973256. The device is classified under product code KPL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JIMMY JOHN III RECTAL NOZZLE?

JIMMY JOHN III RECTAL NOZZLE is a medical device that received FDA 510(k) clearance on 1997-09-29. The listed applicant is Colon Therapeutics. The 510(k) number is K973256.

When did JIMMY JOHN III RECTAL NOZZLE receive FDA 510(k) clearance?

JIMMY JOHN III RECTAL NOZZLE received FDA 510(k) clearance on 1997-09-29, under 510(k) number K973256.

Who is the listed applicant for JIMMY JOHN III RECTAL NOZZLE?

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 RECTAL NOZZLE?

The FDA product code for JIMMY JOHN III RECTAL NOZZLE is KPL.

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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.

K972455JIMMY JOHN III RECTAL NOZZEL, MODEL CITK881720JIMMY JOHN IIIK873948MODIFIED RECTAL NOZZLEK870127MODIFIED JIMMY JOHN IIIK870376JIMMY JOHN III, COLONIC IRRIGATION SYSTEMK860943JIMMY JOHN III, RECTAL NOZZLE (MODIFICATION)

View all 8 devices →

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.

K201861Bio Fluff SystemGnali Bocia S.R.L.K180800Colonic Plus Regular, Small, and Straight Shape HydrokitColonic PlusK152834Colonplus Colonkit small, Colonplus Colonkit large, Colonplus Colonkit with Stop Collar 6, Colonplus Colonkit with Stop Collar 10Colonplus Equipments & Speculums, S.L.K094022THE WATER LILYClearwater Products, LLCK071057COLONIC & ENEMA NOZZLETiller Mind Body, Inc.K051344COLONIC AND ENEMA NOZZLEUltimate Concepts, Inc.

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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