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FDA 510(k)

LIGHTNING DIALYZER

K-Number: K810871 · 1981-07-10

ApplicantClintox Laboratories, Inc.
Decision Date1981-07-10
Product CodeDHY
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LIGHTNING DIALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Clintox Laboratories, Inc.. It received FDA 510(k) clearance on 1981-07-10 under 510(k) number K810871. The device is classified under product code DHY. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHTNING DIALYZER?

LIGHTNING DIALYZER is a medical device that received FDA 510(k) clearance on 1981-07-10. The listed applicant is Clintox Laboratories, Inc.. The 510(k) number is K810871.

When did LIGHTNING DIALYZER receive FDA 510(k) clearance?

LIGHTNING DIALYZER received FDA 510(k) clearance on 1981-07-10, under 510(k) number K810871.

Who is the listed applicant for LIGHTNING DIALYZER?

The FDA 510(k) record lists Clintox Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIGHTNING DIALYZER?

The FDA product code for LIGHTNING DIALYZER is DHY.

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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

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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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