AT EASE ADULT DIAPER
K-Number: K880455 · 1988-04-14
Advertisement
Device Summary
Frequently Asked Questions
What is the AT EASE ADULT DIAPER?
AT EASE ADULT DIAPER is a medical device that received FDA 510(k) clearance on 1988-04-14. The listed applicant is Hospital Specialty Co.. The 510(k) number is K880455.
When did AT EASE ADULT DIAPER receive FDA 510(k) clearance?
AT EASE ADULT DIAPER received FDA 510(k) clearance on 1988-04-14, under 510(k) number K880455.
Who is the listed applicant for AT EASE ADULT DIAPER?
The FDA 510(k) record lists Hospital Specialty Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AT EASE ADULT DIAPER?
The FDA product code for AT EASE ADULT DIAPER is EYQ.
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 Hospital Specialty Co. 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: EYQ)
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.
Advertisement