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FDA 510(k)

LOGIC LAPAROSCOPIC SCISSORS

K-Number: K063485 · 2006-12-01

ApplicantSurgical Innovations Plc
Decision Date2006-12-01
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LOGIC LAPAROSCOPIC SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Innovations Plc. It received FDA 510(k) clearance on 2006-12-01 under 510(k) number K063485. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOGIC LAPAROSCOPIC SCISSORS?

LOGIC LAPAROSCOPIC SCISSORS is a medical device that received FDA 510(k) clearance on 2006-12-01. The listed applicant is Surgical Innovations Plc. The 510(k) number is K063485.

When did LOGIC LAPAROSCOPIC SCISSORS receive FDA 510(k) clearance?

LOGIC LAPAROSCOPIC SCISSORS received FDA 510(k) clearance on 2006-12-01, under 510(k) number K063485.

Who is the listed applicant for LOGIC LAPAROSCOPIC SCISSORS?

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 SCISSORS?

The FDA product code for LOGIC LAPAROSCOPIC SCISSORS is GEI.

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Other records listing Surgical Innovations Plc as applicant

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Related Devices (Code: GEI)

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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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