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FDA 510(k)

BECKMAN ASTRA

K-Number: K822039 · 1982-10-21

ApplicantBeckman Instruments, Inc.
Decision Date1982-10-21
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BECKMAN ASTRA 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 1982-10-21 under 510(k) number K822039. The device is classified under product code JGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECKMAN ASTRA?

BECKMAN ASTRA is a medical device that received FDA 510(k) clearance on 1982-10-21. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K822039.

When did BECKMAN ASTRA receive FDA 510(k) clearance?

BECKMAN ASTRA received FDA 510(k) clearance on 1982-10-21, under 510(k) number K822039.

Who is the listed applicant for BECKMAN ASTRA?

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 ASTRA?

The FDA product code for BECKMAN ASTRA is JGS.

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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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