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FDA 510(k)

SYRINGE PUMP MS2000

K-Number: K880857 · 1988-09-01

ApplicantSmash Ent., Inc.
Decision Date1988-09-01
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYRINGE PUMP MS2000 is the device name listed in this FDA 510(k) record. The listed applicant is Smash Ent., Inc.. It received FDA 510(k) clearance on 1988-09-01 under 510(k) number K880857. 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 PUMP MS2000?

SYRINGE PUMP MS2000 is a medical device that received FDA 510(k) clearance on 1988-09-01. The listed applicant is Smash Ent., Inc.. The 510(k) number is K880857.

When did SYRINGE PUMP MS2000 receive FDA 510(k) clearance?

SYRINGE PUMP MS2000 received FDA 510(k) clearance on 1988-09-01, under 510(k) number K880857.

Who is the listed applicant for SYRINGE PUMP MS2000?

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

What is the FDA product code for SYRINGE PUMP MS2000?

The FDA product code for SYRINGE PUMP MS2000 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 Smash Ent., 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.

K881162ENTERA* ENTERAL FEEDING BAGK880373IONOMETER E-HK AND ACCESSORIESK870183IONOMETER EF AND ACCESSORIES

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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