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FDA 510(k)

SYNCHRON SYSTEMS CANNABINOID 20 NG REAGENT

K-Number: K955677 · 1996-04-03

ApplicantBeckman Instruments, Inc.
Decision Date1996-04-03
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

SYNCHRON SYSTEMS CANNABINOID 20 NG REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1996-04-03 under 510(k) number K955677. The device is classified under product code LDJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNCHRON SYSTEMS CANNABINOID 20 NG REAGENT?

SYNCHRON SYSTEMS CANNABINOID 20 NG REAGENT is a medical device that received FDA 510(k) clearance on 1996-04-03. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K955677.

When did SYNCHRON SYSTEMS CANNABINOID 20 NG REAGENT receive FDA 510(k) clearance?

SYNCHRON SYSTEMS CANNABINOID 20 NG REAGENT received FDA 510(k) clearance on 1996-04-03, under 510(k) number K955677.

Who is the listed applicant for SYNCHRON SYSTEMS CANNABINOID 20 NG REAGENT?

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

What is the FDA product code for SYNCHRON SYSTEMS CANNABINOID 20 NG REAGENT?

The FDA product code for SYNCHRON SYSTEMS CANNABINOID 20 NG REAGENT is LDJ.

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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.

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