URO-BAGGIE
K-Number: K895168 · 1990-03-22
Advertisement
Device Summary
Frequently Asked Questions
What is the URO-BAGGIE?
URO-BAGGIE is a medical device that received FDA 510(k) clearance on 1990-03-22. The listed applicant is Cwt Workshop. The 510(k) number is K895168.
When did URO-BAGGIE receive FDA 510(k) clearance?
URO-BAGGIE received FDA 510(k) clearance on 1990-03-22, under 510(k) number K895168.
Who is the listed applicant for URO-BAGGIE?
The FDA 510(k) record lists Cwt Workshop as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URO-BAGGIE?
The FDA product code for URO-BAGGIE is KNX.
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.
Related Devices (Code: KNX)
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