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FDA 510(k)

DRYTIME FOR POTTY TRAINING

K-Number: K955338 · 1996-03-12

Decision Date1996-03-12
Product CodeKPN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DRYTIME FOR POTTY TRAINING is the device name listed in this FDA 510(k) record. The listed applicant is Health Sense Intl., Inc.. It received FDA 510(k) clearance on 1996-03-12 under 510(k) number K955338. The device is classified under product code KPN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRYTIME FOR POTTY TRAINING?

DRYTIME FOR POTTY TRAINING is a medical device that received FDA 510(k) clearance on 1996-03-12. The listed applicant is Health Sense Intl., Inc.. The 510(k) number is K955338.

When did DRYTIME FOR POTTY TRAINING receive FDA 510(k) clearance?

DRYTIME FOR POTTY TRAINING received FDA 510(k) clearance on 1996-03-12, under 510(k) number K955338.

Who is the listed applicant for DRYTIME FOR POTTY TRAINING?

The FDA 510(k) record lists Health Sense Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRYTIME FOR POTTY TRAINING?

The FDA product code for DRYTIME FOR POTTY TRAINING is KPN.

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 Health Sense Intl., 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: KPN)

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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