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FDA 510(k)

RP-510/RP-514 PARALLEL PLATE DIALYZERS

K-Number: K780427 · 1978-05-19

ApplicantHospal Medical Corp.
Decision Date1978-05-19
Product CodeFJG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RP-510/RP-514 PARALLEL PLATE DIALYZERS 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 1978-05-19 under 510(k) number K780427. The device is classified under product code FJG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RP-510/RP-514 PARALLEL PLATE DIALYZERS?

RP-510/RP-514 PARALLEL PLATE DIALYZERS is a medical device that received FDA 510(k) clearance on 1978-05-19. The listed applicant is Hospal Medical Corp.. The 510(k) number is K780427.

When did RP-510/RP-514 PARALLEL PLATE DIALYZERS receive FDA 510(k) clearance?

RP-510/RP-514 PARALLEL PLATE DIALYZERS received FDA 510(k) clearance on 1978-05-19, under 510(k) number K780427.

Who is the listed applicant for RP-510/RP-514 PARALLEL PLATE DIALYZERS?

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-510/RP-514 PARALLEL PLATE DIALYZERS?

The FDA product code for RP-510/RP-514 PARALLEL PLATE DIALYZERS is FJG.

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Other records listing Hospal Medical Corp. as applicant

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Related Devices (Code: FJG)

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.

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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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