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FDA 510(k)

LIQUICHEK IMMUNOLOGY CONTROL (HUMAN) LEVELS I & II

K-Number: K865014 · 1987-01-09

ApplicantBio-Rad
Decision Date1987-01-09
Product CodeDGR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK IMMUNOLOGY CONTROL (HUMAN) LEVELS I & II is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1987-01-09 under 510(k) number K865014. The device is classified under product code DGR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK IMMUNOLOGY CONTROL (HUMAN) LEVELS I & II?

LIQUICHEK IMMUNOLOGY CONTROL (HUMAN) LEVELS I & II is a medical device that received FDA 510(k) clearance on 1987-01-09. The listed applicant is Bio-Rad. The 510(k) number is K865014.

When did LIQUICHEK IMMUNOLOGY CONTROL (HUMAN) LEVELS I & II receive FDA 510(k) clearance?

LIQUICHEK IMMUNOLOGY CONTROL (HUMAN) LEVELS I & II received FDA 510(k) clearance on 1987-01-09, under 510(k) number K865014.

Who is the listed applicant for LIQUICHEK IMMUNOLOGY CONTROL (HUMAN) LEVELS I & II?

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

What is the FDA product code for LIQUICHEK IMMUNOLOGY CONTROL (HUMAN) LEVELS I & II?

The FDA product code for LIQUICHEK IMMUNOLOGY CONTROL (HUMAN) LEVELS I & II is DGR.

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Related Devices (Code: DGR)

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.

K961544QUALITROL IGAME CONTROLS, LEVELS 1 AND 2Consolidated Technologies, Inc.K902220PRECIPATH(R) IM NORMAL & ABNORMAL IMMUNO. CONTROLBoehringer Mannheim Corp.K790298RADIOASSAY, CONTROL SERUM I, II, IIIKallestad Laboratories, Inc.K781355ICS NORMAL CONTROL SERUMBeckman Instruments, Inc.

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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