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FDA 510(k)

BECKMAN DP-5500 DATA REDUCTION SYSTEM

K-Number: K802594 · 1980-11-12

ApplicantBeckman Instruments, Inc.
Decision Date1980-11-12
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BECKMAN DP-5500 DATA REDUCTION SYSTEM 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 1980-11-12 under 510(k) number K802594. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECKMAN DP-5500 DATA REDUCTION SYSTEM?

BECKMAN DP-5500 DATA REDUCTION SYSTEM is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K802594.

When did BECKMAN DP-5500 DATA REDUCTION SYSTEM receive FDA 510(k) clearance?

BECKMAN DP-5500 DATA REDUCTION SYSTEM received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802594.

Who is the listed applicant for BECKMAN DP-5500 DATA REDUCTION SYSTEM?

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 BECKMAN DP-5500 DATA REDUCTION SYSTEM?

The FDA product code for BECKMAN DP-5500 DATA REDUCTION SYSTEM is JQP.

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Other records listing Beckman Instruments, Inc. as applicant

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Related Devices (Code: JQP)

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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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