FDA 510(k)

I.V. LINK

K-Number: K933366 · 1994-01-10

Decision Date1994-01-10

Product CodeFPO

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

I.V. LINK is the device name listed in this FDA 510(k) record. The listed applicant is Deville Laboratories, Inc.. It received FDA 510(k) clearance on 1994-01-10 under 510(k) number K933366. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.V. LINK?

I.V. LINK is a medical device that received FDA 510(k) clearance on 1994-01-10. The listed applicant is Deville Laboratories, Inc.. The 510(k) number is K933366.

When did I.V. LINK receive FDA 510(k) clearance?

I.V. LINK received FDA 510(k) clearance on 1994-01-10, under 510(k) number K933366.

Who is the listed applicant for I.V. LINK?

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

What is the FDA product code for I.V. LINK?

The FDA product code for I.V. LINK is FPO.

Related Devices (Code: FPO)

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.

K113598POWER-LOAD COT FASTENER SYSTEMStryker Medical K072598IRSG I-MOVER FOR BEDSInternational Retail Services Group, LLC K972528DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)Dyna Corp.K955766ADULT-PEDIATRIC TRANSPORT SYSTEMInternational Biomedical, Inc.K962181HARE MODEL 2000 EZ LOADER MODEL 95555Dyna Corp.K961437WHEELED STRETCHERHill-Rom, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.