LEKSELL IMAGE GUIDANCE SURGICAL SYSTEM (LIGS)
K-Number: K961639 · 1996-07-26
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Device Summary
Frequently Asked Questions
What is the LEKSELL IMAGE GUIDANCE SURGICAL SYSTEM (LIGS)?
LEKSELL IMAGE GUIDANCE SURGICAL SYSTEM (LIGS) is a medical device that received FDA 510(k) clearance on 1996-07-26. The listed applicant is Elekta Instrument AB. The 510(k) number is K961639.
When did LEKSELL IMAGE GUIDANCE SURGICAL SYSTEM (LIGS) receive FDA 510(k) clearance?
LEKSELL IMAGE GUIDANCE SURGICAL SYSTEM (LIGS) received FDA 510(k) clearance on 1996-07-26, under 510(k) number K961639.
Who is the listed applicant for LEKSELL IMAGE GUIDANCE SURGICAL SYSTEM (LIGS)?
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 IMAGE GUIDANCE SURGICAL SYSTEM (LIGS)?
The FDA product code for LEKSELL IMAGE GUIDANCE SURGICAL SYSTEM (LIGS) is HAW.
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: HAW)
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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