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FDA 510(k)

SP55 SYRINGE PUMP

K-Number: K870330 · 1987-06-15

ApplicantVickers , Ltd.
Decision Date1987-06-15
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SP55 SYRINGE PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Vickers , Ltd.. It received FDA 510(k) clearance on 1987-06-15 under 510(k) number K870330. 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 SP55 SYRINGE PUMP?

SP55 SYRINGE PUMP is a medical device that received FDA 510(k) clearance on 1987-06-15. The listed applicant is Vickers , Ltd.. The 510(k) number is K870330.

When did SP55 SYRINGE PUMP receive FDA 510(k) clearance?

SP55 SYRINGE PUMP received FDA 510(k) clearance on 1987-06-15, under 510(k) number K870330.

Who is the listed applicant for SP55 SYRINGE PUMP?

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

What is the FDA product code for SP55 SYRINGE PUMP?

The FDA product code for SP55 SYRINGE 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 Vickers , Ltd. 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.

K870279VP2000 INFUSION PUMPK854597VICKERS MEDICAL MODEL 271 HEART RATE MONITORK854598VICKERS MEDICAL MODEL 272 TEMPERATURE MONITORK854599VICKERS MEDICAL MODEL 273 OXYGEN MONITOR

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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