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FDA 510(k)

LP LATERAL FLUORO POSITIONER (B5077A)

K-Number: K872061 · 1987-06-22

ApplicantGeneral Electric Co.
Decision Date1987-06-22
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LP LATERAL FLUORO POSITIONER (B5077A) is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1987-06-22 under 510(k) number K872061. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LP LATERAL FLUORO POSITIONER (B5077A)?

LP LATERAL FLUORO POSITIONER (B5077A) is a medical device that received FDA 510(k) clearance on 1987-06-22. The listed applicant is General Electric Co.. The 510(k) number is K872061.

When did LP LATERAL FLUORO POSITIONER (B5077A) receive FDA 510(k) clearance?

LP LATERAL FLUORO POSITIONER (B5077A) received FDA 510(k) clearance on 1987-06-22, under 510(k) number K872061.

Who is the listed applicant for LP LATERAL FLUORO POSITIONER (B5077A)?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LP LATERAL FLUORO POSITIONER (B5077A)?

The FDA product code for LP LATERAL FLUORO POSITIONER (B5077A) is JAA.

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Related Devices (Code: JAA)

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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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