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FDA 510(k)

MONITOR, BECKMAN LB-3CO2

K-Number: K782138 · 1979-01-31

ApplicantBeckman Instruments, Inc.
Decision Date1979-01-31
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MONITOR, BECKMAN LB-3CO2 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 1979-01-31 under 510(k) number K782138. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITOR, BECKMAN LB-3CO2?

MONITOR, BECKMAN LB-3CO2 is a medical device that received FDA 510(k) clearance on 1979-01-31. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K782138.

When did MONITOR, BECKMAN LB-3CO2 receive FDA 510(k) clearance?

MONITOR, BECKMAN LB-3CO2 received FDA 510(k) clearance on 1979-01-31, under 510(k) number K782138.

Who is the listed applicant for MONITOR, BECKMAN LB-3CO2?

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 MONITOR, BECKMAN LB-3CO2?

The FDA product code for MONITOR, BECKMAN LB-3CO2 is CCK.

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Related Devices (Code: CCK)

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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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