FDA 510(k)

REAGENT, HDL

K-Number: K781740 · 1978-11-22

Decision Date1978-11-22

Product CodeCHH

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

REAGENT, HDL is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1978-11-22 under 510(k) number K781740. The device is classified under product code CHH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAGENT, HDL?

REAGENT, HDL is a medical device that received FDA 510(k) clearance on 1978-11-22. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K781740.

When did REAGENT, HDL receive FDA 510(k) clearance?

REAGENT, HDL received FDA 510(k) clearance on 1978-11-22, under 510(k) number K781740.

Who is the listed applicant for REAGENT, HDL?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REAGENT, HDL?

The FDA product code for REAGENT, HDL is CHH.

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Other records listing Fisher Scientific Co., LLC as applicant

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Related Devices (Code: CHH)

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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.