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FDA 510(k)

QUIK COLUMN METHODOLOGY

K-Number: K790583 · 1979-04-23

ApplicantHelena Laboratories
Decision Date1979-04-23
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

QUIK COLUMN METHODOLOGY is the device name listed in this FDA 510(k) record. The listed applicant is Helena Laboratories. It received FDA 510(k) clearance on 1979-04-23 under 510(k) number K790583. The device is classified under product code LCP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUIK COLUMN METHODOLOGY?

QUIK COLUMN METHODOLOGY is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Helena Laboratories. The 510(k) number is K790583.

When did QUIK COLUMN METHODOLOGY receive FDA 510(k) clearance?

QUIK COLUMN METHODOLOGY received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790583.

Who is the listed applicant for QUIK COLUMN METHODOLOGY?

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

What is the FDA product code for QUIK COLUMN METHODOLOGY?

The FDA product code for QUIK COLUMN METHODOLOGY is LCP.

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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

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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