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FDA 510(k)

CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY

K-Number: K914510 · 1991-11-19

ApplicantBeckman Instruments, Inc.
Decision Date1991-11-19
Product CodeJFN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY 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 1991-11-19 under 510(k) number K914510. The device is classified under product code JFN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY?

CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY is a medical device that received FDA 510(k) clearance on 1991-11-19. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K914510.

When did CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY receive FDA 510(k) clearance?

CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY received FDA 510(k) clearance on 1991-11-19, under 510(k) number K914510.

Who is the listed applicant for CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY?

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 CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY?

The FDA product code for CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY is JFN.

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Related Devices (Code: JFN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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