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FDA 510(k)

DYNAMIC HOLLOW FIBER DIALYZER DS-SERIES MODEL AS-851

K-Number: K982134 · 1999-04-14

ApplicantDynamic Technology Corp.
Decision Date1999-04-14
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DYNAMIC HOLLOW FIBER DIALYZER DS-SERIES MODEL AS-851 is the device name listed in this FDA 510(k) record. The listed applicant is Dynamic Technology Corp.. It received FDA 510(k) clearance on 1999-04-14 under 510(k) number K982134. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNAMIC HOLLOW FIBER DIALYZER DS-SERIES MODEL AS-851?

DYNAMIC HOLLOW FIBER DIALYZER DS-SERIES MODEL AS-851 is a medical device that received FDA 510(k) clearance on 1999-04-14. The listed applicant is Dynamic Technology Corp.. The 510(k) number is K982134.

When did DYNAMIC HOLLOW FIBER DIALYZER DS-SERIES MODEL AS-851 receive FDA 510(k) clearance?

DYNAMIC HOLLOW FIBER DIALYZER DS-SERIES MODEL AS-851 received FDA 510(k) clearance on 1999-04-14, under 510(k) number K982134.

Who is the listed applicant for DYNAMIC HOLLOW FIBER DIALYZER DS-SERIES MODEL AS-851?

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

What is the FDA product code for DYNAMIC HOLLOW FIBER DIALYZER DS-SERIES MODEL AS-851?

The FDA product code for DYNAMIC HOLLOW FIBER DIALYZER DS-SERIES MODEL AS-851 is KDI.

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Other records listing Dynamic Technology 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.

K011537DYNAMIC HOLLOW FIBER DIALYZER DS-SERIES, MODEL: POLYSULFONE 100 HFS, POLYSULFONE 130 HFSK990159DYNAMIC HOLLOW FIBER DIALYZER DH-SERIES, MODEL AH 90111K973291DYNAMIC HOLLOW FIBER DIALYZER DC-SERIES

Related Devices (Code: KDI)

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.

K261267Careflux H60;Careflux H70;Careflux V500Fresenius Medical Care Renal Therapies Group, LLCK252377NxStage System One with NxViewFresenius Medical Care Renal Therapies Group, LLCK260533ELISIO™-HNipro Medical CorporationK252459multiFlux 130 (F00013123); multiFlux 160 (F00013124)Fresenius Medical Care Renal Therapies Group, LLCK253412Tablo Hemodialysis System (PN-0008000, PN-0006000U)Outset Medical, Inc.K253518FX CorAL 40; FX CorAL 50Fresenius Medical Care Renal Therapies Group, LLC

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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