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FDA 510(k)

CLEARWATER COLON HYDROTHERAPY (DISPOSABLE SPECULUM SPO1 LARGE & SP02 SMALL)

K-Number: K000388 · 2000-08-08

Decision Date2000-08-08
Product CodeKPL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLEARWATER COLON HYDROTHERAPY (DISPOSABLE SPECULUM SPO1 LARGE & SP02 SMALL) is the device name listed in this FDA 510(k) record. The listed applicant is Clearwater Colon Hydrotherapy, Inc.. It received FDA 510(k) clearance on 2000-08-08 under 510(k) number K000388. 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 CLEARWATER COLON HYDROTHERAPY (DISPOSABLE SPECULUM SPO1 LARGE & SP02 SMALL)?

CLEARWATER COLON HYDROTHERAPY (DISPOSABLE SPECULUM SPO1 LARGE & SP02 SMALL) is a medical device that received FDA 510(k) clearance on 2000-08-08. The listed applicant is Clearwater Colon Hydrotherapy, Inc.. The 510(k) number is K000388.

When did CLEARWATER COLON HYDROTHERAPY (DISPOSABLE SPECULUM SPO1 LARGE & SP02 SMALL) receive FDA 510(k) clearance?

CLEARWATER COLON HYDROTHERAPY (DISPOSABLE SPECULUM SPO1 LARGE & SP02 SMALL) received FDA 510(k) clearance on 2000-08-08, under 510(k) number K000388.

Who is the listed applicant for CLEARWATER COLON HYDROTHERAPY (DISPOSABLE SPECULUM SPO1 LARGE & SP02 SMALL)?

The FDA 510(k) record lists Clearwater Colon Hydrotherapy, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEARWATER COLON HYDROTHERAPY (DISPOSABLE SPECULUM SPO1 LARGE & SP02 SMALL)?

The FDA product code for CLEARWATER COLON HYDROTHERAPY (DISPOSABLE SPECULUM SPO1 LARGE & SP02 SMALL) 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 Clearwater Colon Hydrotherapy, 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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