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FDA 510(k)

LATERAL ANGULATING FLUORO SUSPENSION

K-Number: K820184 · 1982-02-24

ApplicantGeneral Electric Co.
Decision Date1982-02-24
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LATERAL ANGULATING FLUORO SUSPENSION 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 1982-02-24 under 510(k) number K820184. 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 LATERAL ANGULATING FLUORO SUSPENSION?

LATERAL ANGULATING FLUORO SUSPENSION is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is General Electric Co.. The 510(k) number is K820184.

When did LATERAL ANGULATING FLUORO SUSPENSION receive FDA 510(k) clearance?

LATERAL ANGULATING FLUORO SUSPENSION received FDA 510(k) clearance on 1982-02-24, under 510(k) number K820184.

Who is the listed applicant for LATERAL ANGULATING FLUORO SUSPENSION?

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 LATERAL ANGULATING FLUORO SUSPENSION?

The FDA product code for LATERAL ANGULATING FLUORO SUSPENSION 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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