FDA 510(k)

CART, INSTRUMENT

K-Number: K880536 · 1988-02-24

Decision Date1988-02-24

Product Code

DecisionSubstantially Equivalent

Device Summary

CART, INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1988-02-24 under 510(k) number K880536. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CART, INSTRUMENT?

CART, INSTRUMENT is a medical device that received FDA 510(k) clearance on 1988-02-24. The listed applicant is Ferguson Medical. The 510(k) number is K880536.

When did CART, INSTRUMENT receive FDA 510(k) clearance?

CART, INSTRUMENT received FDA 510(k) clearance on 1988-02-24, under 510(k) number K880536.

Who is the listed applicant for CART, INSTRUMENT?

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

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.