FDA 510(k)

ELECTROPHORESIS REAGENT SET, HDL

K-Number: K790791 · 1979-06-15

Decision Date1979-06-15

Product CodeLBT

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

ELECTROPHORESIS REAGENT SET, HDL is the device name listed in this FDA 510(k) record. The listed applicant is Gelman Sciences, Inc.. It received FDA 510(k) clearance on 1979-06-15 under 510(k) number K790791. The device is classified under product code LBT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROPHORESIS REAGENT SET, HDL?

ELECTROPHORESIS REAGENT SET, HDL is a medical device that received FDA 510(k) clearance on 1979-06-15. The listed applicant is Gelman Sciences, Inc.. The 510(k) number is K790791.

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

ELECTROPHORESIS REAGENT SET, HDL received FDA 510(k) clearance on 1979-06-15, under 510(k) number K790791.

Who is the listed applicant for ELECTROPHORESIS REAGENT SET, HDL?

The FDA 510(k) record lists Gelman Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROPHORESIS REAGENT SET, HDL?

The FDA product code for ELECTROPHORESIS REAGENT SET, HDL is LBT.

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Related Devices (Code: LBT)

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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.