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FDA 510(k)

VIVUS 50 AND VIVUS 100 PERSONAL INFUSER

K-Number: K915646 · 1992-06-15

ApplicantI-Flow Corp.
Decision Date1992-06-15
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIVUS 50 AND VIVUS 100 PERSONAL INFUSER is the device name listed in this FDA 510(k) record. The listed applicant is I-Flow Corp.. It received FDA 510(k) clearance on 1992-06-15 under 510(k) number K915646. 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 VIVUS 50 AND VIVUS 100 PERSONAL INFUSER?

VIVUS 50 AND VIVUS 100 PERSONAL INFUSER is a medical device that received FDA 510(k) clearance on 1992-06-15. The listed applicant is I-Flow Corp.. The 510(k) number is K915646.

When did VIVUS 50 AND VIVUS 100 PERSONAL INFUSER receive FDA 510(k) clearance?

VIVUS 50 AND VIVUS 100 PERSONAL INFUSER received FDA 510(k) clearance on 1992-06-15, under 510(k) number K915646.

Who is the listed applicant for VIVUS 50 AND VIVUS 100 PERSONAL INFUSER?

The FDA 510(k) record lists I-Flow Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIVUS 50 AND VIVUS 100 PERSONAL INFUSER?

The FDA product code for VIVUS 50 AND VIVUS 100 PERSONAL INFUSER is FRN.

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Other records listing I-Flow Corp. 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.

K063530ON-Q, PAINBUSTER, C-BLOC, SELECT-A-FLOW, ONDEMAND, HOMEPUMP, ECLIPSE, C-SERIES, ONE-STEP KVO, EASYPUMPK063234ON-Q INTRODUCERSK051401ON-Q CATHETER, ON-ANTIMICROBIAL CATHETER, SOAKER CATHETER, I-FLOW CATHETERK052117I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOCK, HOMEPUMP, EASYPUMP)K043456MODIFICATION TO SOAKER CATHETERK040337I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOC, HOMEPUMP)

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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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