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FDA 510(k)

KINEMATIC POSITIONERS

K-Number: K972704 · 1997-09-29

ApplicantGe Medical Systems, Inc.
Decision Date1997-09-29
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KINEMATIC POSITIONERS 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 1997-09-29 under 510(k) number K972704. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINEMATIC POSITIONERS?

KINEMATIC POSITIONERS is a medical device that received FDA 510(k) clearance on 1997-09-29. The listed applicant is Ge Medical Systems, Inc.. The 510(k) number is K972704.

When did KINEMATIC POSITIONERS receive FDA 510(k) clearance?

KINEMATIC POSITIONERS received FDA 510(k) clearance on 1997-09-29, under 510(k) number K972704.

Who is the listed applicant for KINEMATIC POSITIONERS?

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 KINEMATIC POSITIONERS?

The FDA product code for KINEMATIC POSITIONERS is LNH.

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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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