FLEXIBLE URETERONEPHROSOCOPE
K-Number: K924135 · 1993-04-14
Advertisement
Device Summary
Frequently Asked Questions
What is the FLEXIBLE URETERONEPHROSOCOPE?
FLEXIBLE URETERONEPHROSOCOPE is a medical device that received FDA 510(k) clearance on 1993-04-14. The listed applicant is Applied Medical Resources. The 510(k) number is K924135.
When did FLEXIBLE URETERONEPHROSOCOPE receive FDA 510(k) clearance?
FLEXIBLE URETERONEPHROSOCOPE received FDA 510(k) clearance on 1993-04-14, under 510(k) number K924135.
Who is the listed applicant for FLEXIBLE URETERONEPHROSOCOPE?
The FDA 510(k) record lists Applied Medical Resources as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIBLE URETERONEPHROSOCOPE?
The FDA product code for FLEXIBLE URETERONEPHROSOCOPE is FEB.
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 Applied Medical Resources 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: FEB)
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