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FDA 510(k)

TUCK-TITE COLON FLUID RETAINER

K-Number: K833860 · 1983-12-27

ApplicantClayton Medical Products, Inc.
Decision Date1983-12-27
Product CodeFCE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TUCK-TITE COLON FLUID RETAINER is the device name listed in this FDA 510(k) record. The listed applicant is Clayton Medical Products, Inc.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K833860. The device is classified under product code FCE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUCK-TITE COLON FLUID RETAINER?

TUCK-TITE COLON FLUID RETAINER is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Clayton Medical Products, Inc.. The 510(k) number is K833860.

When did TUCK-TITE COLON FLUID RETAINER receive FDA 510(k) clearance?

TUCK-TITE COLON FLUID RETAINER received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833860.

Who is the listed applicant for TUCK-TITE COLON FLUID RETAINER?

The FDA 510(k) record lists Clayton Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TUCK-TITE COLON FLUID RETAINER?

The FDA product code for TUCK-TITE COLON FLUID RETAINER is FCE.

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.

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Other records listing Clayton Medical Products, 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.

K790535CLAYTON COLON CLEANSING KIT

Related Devices (Code: FCE)

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.

K974042AMSURE CLEANSING ENEMA SETAmsino Intl., Inc.K931896PRO-FLO SYSTEMLafayette Pharmacal, Inc.K9223984 SURE TM ENEMA BAG SETBoston Pacific Medical, Inc.K913620ENEMA KITYork County Blind CenterK904534ENEMA BULBR.A.C., Inc.K901182ENEMA BAG SETOrion Life Systems, 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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