Karl Storz Radel Sterilization Trays
K-Number: K203572 · 2021-05-07
Device Summary
Frequently Asked Questions
What is the Karl Storz Radel Sterilization Trays?
Karl Storz Radel Sterilization Trays is a medical device that received FDA 510(k) clearance on 2021-05-07. The listed applicant is Karl Storz Endoscopy America, Inc.. The 510(k) number is K203572.
When did Karl Storz Radel Sterilization Trays receive FDA 510(k) clearance?
Karl Storz Radel Sterilization Trays received FDA 510(k) clearance on 2021-05-07, under 510(k) number K203572.
Who is the listed applicant for Karl Storz Radel Sterilization Trays?
The FDA 510(k) record lists Karl Storz Endoscopy America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Karl Storz Radel Sterilization Trays?
The FDA product code for Karl Storz Radel Sterilization Trays is KCT.
Other records listing Karl Storz Endoscopy America, 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: KCT)
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.