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FDA 510(k)

LEG'MAP OPTION

K-Number: K973270 · 1997-11-25

ApplicantGe Medical Systems, Inc.
Decision Date1997-11-25
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LEG'MAP OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems, Inc.. It received FDA 510(k) clearance on 1997-11-25 under 510(k) number K973270. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEG'MAP OPTION?

LEG'MAP OPTION is a medical device that received FDA 510(k) clearance on 1997-11-25. The listed applicant is Ge Medical Systems, Inc.. The 510(k) number is K973270.

When did LEG'MAP OPTION receive FDA 510(k) clearance?

LEG'MAP OPTION received FDA 510(k) clearance on 1997-11-25, under 510(k) number K973270.

Who is the listed applicant for LEG'MAP OPTION?

The FDA 510(k) record lists Ge Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEG'MAP OPTION?

The FDA product code for LEG'MAP OPTION is IZI.

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Related Devices (Code: IZI)

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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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