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FDA 510(k)

RP-610 PARALLEL PLATE DIALYZER

K-Number: K790827 · 1979-09-04

Decision Date1979-09-04
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RP-610 PARALLEL PLATE DIALYZER 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 1979-09-04 under 510(k) number K790827. 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 RP-610 PARALLEL PLATE DIALYZER?

RP-610 PARALLEL PLATE DIALYZER is a medical device that received FDA 510(k) clearance on 1979-09-04. The listed applicant is Hospal Medical Corp.. The 510(k) number is K790827.

When did RP-610 PARALLEL PLATE DIALYZER receive FDA 510(k) clearance?

RP-610 PARALLEL PLATE DIALYZER received FDA 510(k) clearance on 1979-09-04, under 510(k) number K790827.

Who is the listed applicant for RP-610 PARALLEL PLATE DIALYZER?

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 RP-610 PARALLEL PLATE DIALYZER?

The FDA product code for RP-610 PARALLEL PLATE DIALYZER is KDI.

Related Clinical Trials

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.

Other records listing Hospal Medical 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.

View all 55 devices →

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.

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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