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FDA 510(k)

INFUSA T SYRINGE INFUSION PUMP

K-Number: K904923 · 1991-09-06

ApplicantFerguson Medical
Decision Date1991-09-06
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUSA T 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 1991-09-06 under 510(k) number K904923. 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 T SYRINGE INFUSION PUMP?

INFUSA T SYRINGE INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1991-09-06. The listed applicant is Ferguson Medical. The 510(k) number is K904923.

When did INFUSA T SYRINGE INFUSION PUMP receive FDA 510(k) clearance?

INFUSA T SYRINGE INFUSION PUMP received FDA 510(k) clearance on 1991-09-06, under 510(k) number K904923.

Who is the listed applicant for INFUSA T 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 T SYRINGE INFUSION PUMP?

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

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Related Devices (Code: FRN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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