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FDA 510(k)

LYPHOCHEK MATERNAL SERUM CONTROL, MODEL 220

K-Number: K984594 · 1999-02-02

ApplicantBio-Rad
Decision Date1999-02-02
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LYPHOCHEK MATERNAL SERUM CONTROL, MODEL 220 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1999-02-02 under 510(k) number K984594. 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 LYPHOCHEK MATERNAL SERUM CONTROL, MODEL 220?

LYPHOCHEK MATERNAL SERUM CONTROL, MODEL 220 is a medical device that received FDA 510(k) clearance on 1999-02-02. The listed applicant is Bio-Rad. The 510(k) number is K984594.

When did LYPHOCHEK MATERNAL SERUM CONTROL, MODEL 220 receive FDA 510(k) clearance?

LYPHOCHEK MATERNAL SERUM CONTROL, MODEL 220 received FDA 510(k) clearance on 1999-02-02, under 510(k) number K984594.

Who is the listed applicant for LYPHOCHEK MATERNAL SERUM CONTROL, MODEL 220?

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 LYPHOCHEK MATERNAL SERUM CONTROL, MODEL 220?

The FDA product code for LYPHOCHEK MATERNAL SERUM CONTROL, MODEL 220 is JJY.

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Other records listing Bio-Rad as applicant

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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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