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FDA 510(k)

DIALYSIS MIXING & HOLDING TANK

K-Number: K961416 · 1996-08-21

ApplicantDial Medical Supply
Decision Date1996-08-21
Product CodeFIN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIALYSIS MIXING & HOLDING TANK is the device name listed in this FDA 510(k) record. The listed applicant is Dial Medical Supply. It received FDA 510(k) clearance on 1996-08-21 under 510(k) number K961416. The device is classified under product code FIN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIALYSIS MIXING & HOLDING TANK?

DIALYSIS MIXING & HOLDING TANK is a medical device that received FDA 510(k) clearance on 1996-08-21. The listed applicant is Dial Medical Supply. The 510(k) number is K961416.

When did DIALYSIS MIXING & HOLDING TANK receive FDA 510(k) clearance?

DIALYSIS MIXING & HOLDING TANK received FDA 510(k) clearance on 1996-08-21, under 510(k) number K961416.

Who is the listed applicant for DIALYSIS MIXING & HOLDING TANK?

The FDA 510(k) record lists Dial Medical Supply as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIALYSIS MIXING & HOLDING TANK?

The FDA product code for DIALYSIS MIXING & HOLDING TANK is FIN.

Related Clinical Trials

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Related Devices (Code: FIN)

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.

K112427BICARB MIXING AND DISTRIBUTION SYSTEMIsopure, Corp.K093641TANGO3 WATER STORAGE TANK WITH OZONE DISINFECTION SYSTEMTango3, LLCK060333DIALYSIS SERVICES, INC., TYPHOON BICARB MIXING AND DISTRIBUTION SYSTEMDialysis Services, Inc.K051031AMERIWATER SOLUTION MIX AND DISTRIBUTION SYSTEM FOR HEMODIALYSISAmeriwaterK031502USFILTER BICARBONATE MIXING AND DISPENSING (BICARB) SYSTEMUsfilterK033118BIPRO MODEL SDS-CB200Medical Solutions International

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.

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