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FDA 510(k)

ACCULAB SUPPLIES CHEMICAL ANALYZERS

K-Number: K840501 · 1984-04-04

Decision Date1984-04-04
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACCULAB SUPPLIES CHEMICAL ANALYZERS is the device name listed in this FDA 510(k) record. The listed applicant is Precision Technology, Inc.. It received FDA 510(k) clearance on 1984-04-04 under 510(k) number K840501. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCULAB SUPPLIES CHEMICAL ANALYZERS?

ACCULAB SUPPLIES CHEMICAL ANALYZERS is a medical device that received FDA 510(k) clearance on 1984-04-04. The listed applicant is Precision Technology, Inc.. The 510(k) number is K840501.

When did ACCULAB SUPPLIES CHEMICAL ANALYZERS receive FDA 510(k) clearance?

ACCULAB SUPPLIES CHEMICAL ANALYZERS received FDA 510(k) clearance on 1984-04-04, under 510(k) number K840501.

Who is the listed applicant for ACCULAB SUPPLIES CHEMICAL ANALYZERS?

The FDA 510(k) record lists Precision Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCULAB SUPPLIES CHEMICAL ANALYZERS?

The FDA product code for ACCULAB SUPPLIES CHEMICAL ANALYZERS is JJE.

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 Precision Technology, 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.

Related Devices (Code: JJE)

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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