FDA 510(k)

3100 INFUSION PUMP

K-Number: K912192 · 1992-02-14

Decision Date1992-02-14

Product CodeFRN

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

3100 INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Graseby Medical , Ltd.. It received FDA 510(k) clearance on 1992-02-14 under 510(k) number K912192. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3100 INFUSION PUMP?

3100 INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1992-02-14. The listed applicant is Graseby Medical , Ltd.. The 510(k) number is K912192.

When did 3100 INFUSION PUMP receive FDA 510(k) clearance?

3100 INFUSION PUMP received FDA 510(k) clearance on 1992-02-14, under 510(k) number K912192.

Who is the listed applicant for 3100 INFUSION PUMP?

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

What is the FDA product code for 3100 INFUSION PUMP?

The FDA product code for 3100 INFUSION PUMP is FRN.

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Other records listing Graseby Medical , Ltd. as applicant

K9447219000 INFUSION PUMP K9313183400 INFUSION PUMP K915270PATIENT CONTROLLED SYRINGE PUMP TYPE 3300 K9121933000 INFUSION PUMP

Related Devices (Code: FRN)

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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.