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FDA 510(k)

SYNCHRON CX3

K-Number: K864236 · 1986-12-31

ApplicantBeckman Instruments, Inc.
Decision Date1986-12-31
Product CodeJJF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SYNCHRON CX3 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 1986-12-31 under 510(k) number K864236. The device is classified under product code JJF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNCHRON CX3?

SYNCHRON CX3 is a medical device that received FDA 510(k) clearance on 1986-12-31. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K864236.

When did SYNCHRON CX3 receive FDA 510(k) clearance?

SYNCHRON CX3 received FDA 510(k) clearance on 1986-12-31, under 510(k) number K864236.

Who is the listed applicant for SYNCHRON CX3?

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 CX3?

The FDA product code for SYNCHRON CX3 is JJF.

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Other records listing Beckman Instruments, Inc. as applicant

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Related Devices (Code: JJF)

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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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