LEKSELL GAMMAPLAN
K-Number: K061540 · 2006-07-05
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Device Summary
Frequently Asked Questions
What is the LEKSELL GAMMAPLAN?
LEKSELL GAMMAPLAN is a medical device that received FDA 510(k) clearance on 2006-07-05. The listed applicant is Elekta Instrument AB. The 510(k) number is K061540.
When did LEKSELL GAMMAPLAN receive FDA 510(k) clearance?
LEKSELL GAMMAPLAN received FDA 510(k) clearance on 2006-07-05, under 510(k) number K061540.
Who is the listed applicant for LEKSELL GAMMAPLAN?
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 GAMMAPLAN?
The FDA product code for LEKSELL GAMMAPLAN 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.
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