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FDA 510(k)

INFUSA D.SLT SYRINGE INFUSION PUMP

K-Number: K904922 · 1991-09-04

ApplicantFerguson Medical
Decision Date1991-09-04
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUSA D.SLT SYRINGE INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1991-09-04 under 510(k) number K904922. 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 INFUSA D.SLT SYRINGE INFUSION PUMP?

INFUSA D.SLT SYRINGE INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1991-09-04. The listed applicant is Ferguson Medical. The 510(k) number is K904922.

When did INFUSA D.SLT SYRINGE INFUSION PUMP receive FDA 510(k) clearance?

INFUSA D.SLT SYRINGE INFUSION PUMP received FDA 510(k) clearance on 1991-09-04, under 510(k) number K904922.

Who is the listed applicant for INFUSA D.SLT SYRINGE INFUSION PUMP?

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

What is the FDA product code for INFUSA D.SLT SYRINGE INFUSION PUMP?

The FDA product code for INFUSA D.SLT SYRINGE INFUSION PUMP is FRN.

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Related Devices (Code: FRN)

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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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