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FDA 510(k)

PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II

K-Number: K992921 · 1999-11-12

ApplicantPrimus Corp.
Decision Date1999-11-12
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II is the device name listed in this FDA 510(k) record. The listed applicant is Primus Corp.. It received FDA 510(k) clearance on 1999-11-12 under 510(k) number K992921. 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 PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II?

PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II is a medical device that received FDA 510(k) clearance on 1999-11-12. The listed applicant is Primus Corp.. The 510(k) number is K992921.

When did PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II receive FDA 510(k) clearance?

PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II received FDA 510(k) clearance on 1999-11-12, under 510(k) number K992921.

Who is the listed applicant for PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II?

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

What is the FDA product code for PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II?

The FDA product code for PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II is LCP.

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Other records listing Primus 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.

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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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