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FDA 510(k)

LYOPHILIZED G-HB QUIK COLUMN CONTROL

K-Number: K791135 · 1979-06-28

ApplicantHelena Laboratories
Decision Date1979-06-28
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LYOPHILIZED G-HB QUIK COLUMN CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Helena Laboratories. It received FDA 510(k) clearance on 1979-06-28 under 510(k) number K791135. 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 LYOPHILIZED G-HB QUIK COLUMN CONTROL?

LYOPHILIZED G-HB QUIK COLUMN CONTROL is a medical device that received FDA 510(k) clearance on 1979-06-28. The listed applicant is Helena Laboratories. The 510(k) number is K791135.

When did LYOPHILIZED G-HB QUIK COLUMN CONTROL receive FDA 510(k) clearance?

LYOPHILIZED G-HB QUIK COLUMN CONTROL received FDA 510(k) clearance on 1979-06-28, under 510(k) number K791135.

Who is the listed applicant for LYOPHILIZED G-HB QUIK COLUMN CONTROL?

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 LYOPHILIZED G-HB QUIK COLUMN CONTROL?

The FDA product code for LYOPHILIZED G-HB QUIK COLUMN CONTROL is LCP.

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Related Devices (Code: LCP)

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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