PTW DAVID IMRT QC VERIFICATION SYSTEM
K-Number: K062817 · 2006-11-22
Advertisement
Device Summary
Frequently Asked Questions
What is the PTW DAVID IMRT QC VERIFICATION SYSTEM?
PTW DAVID IMRT QC VERIFICATION SYSTEM is a medical device that received FDA 510(k) clearance on 2006-11-22. The listed applicant is Ptw-New York Corp.. The 510(k) number is K062817.
When did PTW DAVID IMRT QC VERIFICATION SYSTEM receive FDA 510(k) clearance?
PTW DAVID IMRT QC VERIFICATION SYSTEM received FDA 510(k) clearance on 2006-11-22, under 510(k) number K062817.
Who is the listed applicant for PTW DAVID IMRT QC VERIFICATION SYSTEM?
The FDA 510(k) record lists Ptw-New York Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PTW DAVID IMRT QC VERIFICATION SYSTEM?
The FDA product code for PTW DAVID IMRT QC VERIFICATION SYSTEM is IYE.
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 Ptw-New York Corp. 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: IYE)
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