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FDA 510(k)

TOILET TRAINER FOR HANDICAPPED CHILD

K-Number: K791423 · 1979-08-10

Decision Date1979-08-10
Product CodeILS
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TOILET TRAINER FOR HANDICAPPED CHILD is the device name listed in this FDA 510(k) record. The listed applicant is Kaye Products, Inc.. It received FDA 510(k) clearance on 1979-08-10 under 510(k) number K791423. The device is classified under product code ILS. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOILET TRAINER FOR HANDICAPPED CHILD?

TOILET TRAINER FOR HANDICAPPED CHILD is a medical device that received FDA 510(k) clearance on 1979-08-10. The listed applicant is Kaye Products, Inc.. The 510(k) number is K791423.

When did TOILET TRAINER FOR HANDICAPPED CHILD receive FDA 510(k) clearance?

TOILET TRAINER FOR HANDICAPPED CHILD received FDA 510(k) clearance on 1979-08-10, under 510(k) number K791423.

Who is the listed applicant for TOILET TRAINER FOR HANDICAPPED CHILD?

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

What is the FDA product code for TOILET TRAINER FOR HANDICAPPED CHILD?

The FDA product code for TOILET TRAINER FOR HANDICAPPED CHILD is ILS.

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 Kaye 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.

View all 12 devices →

Related Devices (Code: ILS)

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

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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