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FDA 510(k)

LOCKBOX FOR USE WITH CADD SOLIS INFUSION PUMP

K-Number: K080743 · 2008-04-25

ApplicantSmiths Medical MD, Inc.
Decision Date2008-04-25
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LOCKBOX FOR USE WITH CADD SOLIS INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Smiths Medical MD, Inc.. It received FDA 510(k) clearance on 2008-04-25 under 510(k) number K080743. 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 LOCKBOX FOR USE WITH CADD SOLIS INFUSION PUMP?

LOCKBOX FOR USE WITH CADD SOLIS INFUSION PUMP is a medical device that received FDA 510(k) clearance on 2008-04-25. The listed applicant is Smiths Medical MD, Inc.. The 510(k) number is K080743.

When did LOCKBOX FOR USE WITH CADD SOLIS INFUSION PUMP receive FDA 510(k) clearance?

LOCKBOX FOR USE WITH CADD SOLIS INFUSION PUMP received FDA 510(k) clearance on 2008-04-25, under 510(k) number K080743.

Who is the listed applicant for LOCKBOX FOR USE WITH CADD SOLIS INFUSION PUMP?

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

What is the FDA product code for LOCKBOX FOR USE WITH CADD SOLIS INFUSION PUMP?

The FDA product code for LOCKBOX FOR USE WITH CADD SOLIS INFUSION PUMP is FRN.

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Other records listing Smiths Medical MD, 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.

K112407SMITH MEDICAL PEEL-AWAY SHEATH INTRODUCERSK111386MEDFUSION MODEL 4000 SYRINGE INFUSION PUMP, PHARMGUARD TOOLBOX 2 MEDICATION SAFETY SOFTWARE AND SUPPORTED SYRINGES (PSS)K101180GRIPPER MICRO BLUNT CANNULA, NON-CORING SAFETY NEEDLE (GRIPPER MICRO NEEDLE) MODEL: 21-3253-24, 21-3258-24, 21-3262-24,K091181LOCKBOX FOR USE WITH MEDFUSION 3000 SERIES PUMPSK082783CADD -SOLIS MEDICATION SAFETY SOFTWARE: ADMINISTRATOR AND POINT-OF-CAREK081156CADD MEDICATION CASSETTE RESERVOIR

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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.

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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