FDA 510(k)

SYNCHON CX DELTA CLIN SYST (CX4, CX5, CX7 DELTA)

K-Number: K950958 · 1995-05-08

Decision Date1995-05-08

Product CodeJJE

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

SYNCHON CX DELTA CLIN SYST (CX4, CX5, CX7 DELTA) 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 1995-05-08 under 510(k) number K950958. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNCHON CX DELTA CLIN SYST (CX4, CX5, CX7 DELTA)?

SYNCHON CX DELTA CLIN SYST (CX4, CX5, CX7 DELTA) is a medical device that received FDA 510(k) clearance on 1995-05-08. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K950958.

When did SYNCHON CX DELTA CLIN SYST (CX4, CX5, CX7 DELTA) receive FDA 510(k) clearance?

SYNCHON CX DELTA CLIN SYST (CX4, CX5, CX7 DELTA) received FDA 510(k) clearance on 1995-05-08, under 510(k) number K950958.

Who is the listed applicant for SYNCHON CX DELTA CLIN SYST (CX4, CX5, CX7 DELTA)?

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 SYNCHON CX DELTA CLIN SYST (CX4, CX5, CX7 DELTA)?

The FDA product code for SYNCHON CX DELTA CLIN SYST (CX4, CX5, CX7 DELTA) is JJE.

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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.