LOGIC LAPAROSCOPIC INSTRUMENT SYSTEM
K-Number: K111986 · 2012-01-26
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Device Summary
Frequently Asked Questions
What is the LOGIC LAPAROSCOPIC INSTRUMENT SYSTEM?
LOGIC LAPAROSCOPIC INSTRUMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2012-01-26. The listed applicant is Surgical Innovations Plc. The 510(k) number is K111986.
When did LOGIC LAPAROSCOPIC INSTRUMENT SYSTEM receive FDA 510(k) clearance?
LOGIC LAPAROSCOPIC INSTRUMENT SYSTEM received FDA 510(k) clearance on 2012-01-26, under 510(k) number K111986.
Who is the listed applicant for LOGIC LAPAROSCOPIC INSTRUMENT SYSTEM?
The FDA 510(k) record lists Surgical Innovations Plc as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOGIC LAPAROSCOPIC INSTRUMENT SYSTEM?
The FDA product code for LOGIC LAPAROSCOPIC INSTRUMENT SYSTEM is GEI.
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 Surgical Innovations Plc 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: GEI)
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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