FDA 510(k)

LIQUICHEK TORCH PLUS IGM CONTROL

K-Number: K040822 · 2004-05-19

Decision Date2004-05-19

Product CodeJJY

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

LIQUICHEK TORCH PLUS IGM CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad Laboratories, Inc.. It received FDA 510(k) clearance on 2004-05-19 under 510(k) number K040822. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK TORCH PLUS IGM CONTROL?

LIQUICHEK TORCH PLUS IGM CONTROL is a medical device that received FDA 510(k) clearance on 2004-05-19. The listed applicant is Bio-Rad Laboratories, Inc.. The 510(k) number is K040822.

When did LIQUICHEK TORCH PLUS IGM CONTROL receive FDA 510(k) clearance?

LIQUICHEK TORCH PLUS IGM CONTROL received FDA 510(k) clearance on 2004-05-19, under 510(k) number K040822.

Who is the listed applicant for LIQUICHEK TORCH PLUS IGM CONTROL?

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

What is the FDA product code for LIQUICHEK TORCH PLUS IGM CONTROL?

The FDA product code for LIQUICHEK TORCH PLUS IGM CONTROL is JJY.

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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.