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FDA 510(k)

H1210

K-Number: K830647 · 1983-03-29

ApplicantHospal Medical Corp.
Decision Date1983-03-29
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

H1210 is the device name listed in this FDA 510(k) record. The listed applicant is Hospal Medical Corp.. It received FDA 510(k) clearance on 1983-03-29 under 510(k) number K830647. 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 H1210?

H1210 is a medical device that received FDA 510(k) clearance on 1983-03-29. The listed applicant is Hospal Medical Corp.. The 510(k) number is K830647.

When did H1210 receive FDA 510(k) clearance?

H1210 received FDA 510(k) clearance on 1983-03-29, under 510(k) number K830647.

Who is the listed applicant for H1210?

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

What is the FDA product code for H1210?

The FDA product code for H1210 is KDI.

Other records listing Hospal Medical Corp. as applicant

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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

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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