LEKSELL GAMMA KNIFE PERFEXION, MODEL 715000
K-Number: K061941 · 2006-08-21
Advertisement
Device Summary
Frequently Asked Questions
What is the LEKSELL GAMMA KNIFE PERFEXION, MODEL 715000?
LEKSELL GAMMA KNIFE PERFEXION, MODEL 715000 is a medical device that received FDA 510(k) clearance on 2006-08-21. The listed applicant is Elekta Instrument AB. The 510(k) number is K061941.
When did LEKSELL GAMMA KNIFE PERFEXION, MODEL 715000 receive FDA 510(k) clearance?
LEKSELL GAMMA KNIFE PERFEXION, MODEL 715000 received FDA 510(k) clearance on 2006-08-21, under 510(k) number K061941.
Who is the listed applicant for LEKSELL GAMMA KNIFE PERFEXION, MODEL 715000?
The FDA 510(k) record lists Elekta Instrument AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEKSELL GAMMA KNIFE PERFEXION, MODEL 715000?
The FDA product code for LEKSELL GAMMA KNIFE PERFEXION, MODEL 715000 is IWB.
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 Elekta Instrument AB 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: IWB)
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