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FDA 510(k)

BECKMAN ASTRA SYSTEM

K-Number: K781442 · 1978-10-03

ApplicantBeckman Instruments, Inc.
Decision Date1978-10-03
Product CodeJJF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BECKMAN ASTRA 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 1978-10-03 under 510(k) number K781442. The device is classified under product code JJF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECKMAN ASTRA SYSTEM?

BECKMAN ASTRA SYSTEM is a medical device that received FDA 510(k) clearance on 1978-10-03. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K781442.

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

BECKMAN ASTRA SYSTEM received FDA 510(k) clearance on 1978-10-03, under 510(k) number K781442.

Who is the listed applicant for BECKMAN ASTRA 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 ASTRA SYSTEM?

The FDA product code for BECKMAN ASTRA SYSTEM is JJF.

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Other records listing Beckman Instruments, Inc. as applicant

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Related Devices (Code: JJF)

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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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