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FDA 510(k)

ACCU-PREP PROGRAMMABLE AUTO-DILUTER

K-Number: K832809 · 1983-10-27

Decision Date1983-10-27
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACCU-PREP PROGRAMMABLE AUTO-DILUTER 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 1983-10-27 under 510(k) number K832809. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCU-PREP PROGRAMMABLE AUTO-DILUTER?

ACCU-PREP PROGRAMMABLE AUTO-DILUTER is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K832809.

When did ACCU-PREP PROGRAMMABLE AUTO-DILUTER receive FDA 510(k) clearance?

ACCU-PREP PROGRAMMABLE AUTO-DILUTER received FDA 510(k) clearance on 1983-10-27, under 510(k) number K832809.

Who is the listed applicant for ACCU-PREP PROGRAMMABLE AUTO-DILUTER?

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 ACCU-PREP PROGRAMMABLE AUTO-DILUTER?

The FDA product code for ACCU-PREP PROGRAMMABLE AUTO-DILUTER is JQW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Beckman Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 281 devices →

Related Devices (Code: JQW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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