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FDA 510(k)

PROMINJECT PROGRAMMABLE INFUSION PUMP

K-Number: K850669 · 1985-04-09

ApplicantPharmacia, Inc.
Decision Date1985-04-09
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROMINJECT PROGRAMMABLE INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1985-04-09 under 510(k) number K850669. 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 PROMINJECT PROGRAMMABLE INFUSION PUMP?

PROMINJECT PROGRAMMABLE INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1985-04-09. The listed applicant is Pharmacia, Inc.. The 510(k) number is K850669.

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

PROMINJECT PROGRAMMABLE INFUSION PUMP received FDA 510(k) clearance on 1985-04-09, under 510(k) number K850669.

Who is the listed applicant for PROMINJECT PROGRAMMABLE INFUSION PUMP?

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

What is the FDA product code for PROMINJECT PROGRAMMABLE INFUSION PUMP?

The FDA product code for PROMINJECT PROGRAMMABLE INFUSION PUMP is FRN.

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Other records listing Pharmacia, Inc. as applicant

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K974350ALLERGAN IMMUNO CAP M4, M8, K70K972364UNICAP PHADIATOPK972068UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82K970420MASTERCAP AM 5.0/MASTERCAP RM 5.0K964152UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMHK962274UNICAP 100

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Related Devices (Code: FRN)

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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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