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FDA 510(k)

BILIRUBIN CALIBRATOR CONTROL

K-Number: K791141 · 1979-08-10

ApplicantBeckman Instruments, Inc.
Decision Date1979-08-10
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BILIRUBIN CALIBRATOR CONTROL 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 1979-08-10 under 510(k) number K791141. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BILIRUBIN CALIBRATOR CONTROL?

BILIRUBIN CALIBRATOR CONTROL is a medical device that received FDA 510(k) clearance on 1979-08-10. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K791141.

When did BILIRUBIN CALIBRATOR CONTROL receive FDA 510(k) clearance?

BILIRUBIN CALIBRATOR CONTROL received FDA 510(k) clearance on 1979-08-10, under 510(k) number K791141.

Who is the listed applicant for BILIRUBIN CALIBRATOR CONTROL?

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 BILIRUBIN CALIBRATOR CONTROL?

The FDA product code for BILIRUBIN CALIBRATOR CONTROL is JJX.

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Other records listing Beckman Instruments, Inc. as applicant

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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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