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FDA 510(k)

THE F SPOON HAND HELD FLUOROSCOPIC COMPRESSION

K-Number: K871911 · 1987-05-29

ApplicantF. Spoon Co.
Decision Date1987-05-29
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THE F SPOON HAND HELD FLUOROSCOPIC COMPRESSION is the device name listed in this FDA 510(k) record. The listed applicant is F. Spoon Co.. It received FDA 510(k) clearance on 1987-05-29 under 510(k) number K871911. 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 THE F SPOON HAND HELD FLUOROSCOPIC COMPRESSION?

THE F SPOON HAND HELD FLUOROSCOPIC COMPRESSION is a medical device that received FDA 510(k) clearance on 1987-05-29. The listed applicant is F. Spoon Co.. The 510(k) number is K871911.

When did THE F SPOON HAND HELD FLUOROSCOPIC COMPRESSION receive FDA 510(k) clearance?

THE F SPOON HAND HELD FLUOROSCOPIC COMPRESSION received FDA 510(k) clearance on 1987-05-29, under 510(k) number K871911.

Who is the listed applicant for THE F SPOON HAND HELD FLUOROSCOPIC COMPRESSION?

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

What is the FDA product code for THE F SPOON HAND HELD FLUOROSCOPIC COMPRESSION?

The FDA product code for THE F SPOON HAND HELD FLUOROSCOPIC COMPRESSION is 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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