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FDA 510(k)

BECKMAN R.PR CONTROL SERUM SET

K-Number: K812425 · 1981-09-23

ApplicantBeckman Instruments, Inc.
Decision Date1981-09-23
Product CodeGMP
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BECKMAN R.PR CONTROL SERUM SET 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 1981-09-23 under 510(k) number K812425. The device is classified under product code GMP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECKMAN R.PR CONTROL SERUM SET?

BECKMAN R.PR CONTROL SERUM SET is a medical device that received FDA 510(k) clearance on 1981-09-23. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K812425.

When did BECKMAN R.PR CONTROL SERUM SET receive FDA 510(k) clearance?

BECKMAN R.PR CONTROL SERUM SET received FDA 510(k) clearance on 1981-09-23, under 510(k) number K812425.

Who is the listed applicant for BECKMAN R.PR CONTROL SERUM SET?

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 R.PR CONTROL SERUM SET?

The FDA product code for BECKMAN R.PR CONTROL SERUM SET is GMP.

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Related Devices (Code: GMP)

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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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