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FDA 510(k)

QUANTIMUNE HFSH RIA HUMAN FOLLICLE-

K-Number: K831742 · 1983-07-18

ApplicantBio-Rad
Decision Date1983-07-18
Product CodeCGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUANTIMUNE HFSH RIA HUMAN FOLLICLE- is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1983-07-18 under 510(k) number K831742. The device is classified under product code CGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTIMUNE HFSH RIA HUMAN FOLLICLE-?

QUANTIMUNE HFSH RIA HUMAN FOLLICLE- is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is Bio-Rad. The 510(k) number is K831742.

When did QUANTIMUNE HFSH RIA HUMAN FOLLICLE- receive FDA 510(k) clearance?

QUANTIMUNE HFSH RIA HUMAN FOLLICLE- received FDA 510(k) clearance on 1983-07-18, under 510(k) number K831742.

Who is the listed applicant for QUANTIMUNE HFSH RIA HUMAN FOLLICLE-?

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 QUANTIMUNE HFSH RIA HUMAN FOLLICLE-?

The FDA product code for QUANTIMUNE HFSH RIA HUMAN FOLLICLE- is CGJ.

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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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