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FDA 510(k)

SYRINGE INFUSION PUMP

K-Number: K791729 · 1979-10-01

ApplicantPrinceton Medical Instruments, Inc.
Decision Date1979-10-01
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYRINGE INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Princeton Medical Instruments, Inc.. It received FDA 510(k) clearance on 1979-10-01 under 510(k) number K791729. 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 SYRINGE INFUSION PUMP?

SYRINGE INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1979-10-01. The listed applicant is Princeton Medical Instruments, Inc.. The 510(k) number is K791729.

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

SYRINGE INFUSION PUMP received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791729.

Who is the listed applicant for SYRINGE INFUSION PUMP?

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

What is the FDA product code for SYRINGE INFUSION PUMP?

The FDA product code for SYRINGE INFUSION PUMP is FRN.

Related Clinical Trials

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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Other records listing Princeton Medical Instruments, Inc. as applicant

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.

K802400MS 16 SYRINGE DRIVER

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.

K253703RemunityPRO+ Pump for Remodulin® (treprostinil) InjectionDeka R&D CorpK252015FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate TubingKoru Medical Systems, Inc.K251636Spectrum IQ Infusion System with Dose IQ Safety Software (3570009)Baxter Healthcare CorporationK251640SIGMA Spectrum Infusion Pump with Master Drug LibraryBaxter Healthcare CorporationK242752MRidium 3870 MRI Infusion Pump System (3870)Iradimed CorporationK243855BD Alaris Infusion System with Guardrails Suite MXCarefusion 303, Inc.

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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