FDA 510(k)

MODEL OSP, SANDHILL AMS

K-Number: K904231 · 1991-01-02

Decision Date1991-01-02

Product CodeFAD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MODEL OSP, SANDHILL AMS is the device name listed in this FDA 510(k) record. The listed applicant is Sandhill Scientific, Inc.. It received FDA 510(k) clearance on 1991-01-02 under 510(k) number K904231. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL OSP, SANDHILL AMS?

MODEL OSP, SANDHILL AMS is a medical device that received FDA 510(k) clearance on 1991-01-02. The listed applicant is Sandhill Scientific, Inc.. The 510(k) number is K904231.

When did MODEL OSP, SANDHILL AMS receive FDA 510(k) clearance?

MODEL OSP, SANDHILL AMS received FDA 510(k) clearance on 1991-01-02, under 510(k) number K904231.

Who is the listed applicant for MODEL OSP, SANDHILL AMS?

The FDA 510(k) record lists Sandhill Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL OSP, SANDHILL AMS?

The FDA product code for MODEL OSP, SANDHILL AMS is FAD.

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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.