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FDA 510(k)

QUANTUM II YEAST IDENT. SYSTEM

K-Number: K832406 · 1983-09-26

ApplicantAbbott Laboratories
Decision Date1983-09-26
Product CodeJXC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

QUANTUM II YEAST IDENT. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1983-09-26 under 510(k) number K832406. The device is classified under product code JXC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTUM II YEAST IDENT. SYSTEM?

QUANTUM II YEAST IDENT. SYSTEM is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Abbott Laboratories. The 510(k) number is K832406.

When did QUANTUM II YEAST IDENT. SYSTEM receive FDA 510(k) clearance?

QUANTUM II YEAST IDENT. SYSTEM received FDA 510(k) clearance on 1983-09-26, under 510(k) number K832406.

Who is the listed applicant for QUANTUM II YEAST IDENT. SYSTEM?

The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUANTUM II YEAST IDENT. SYSTEM?

The FDA product code for QUANTUM II YEAST IDENT. SYSTEM is JXC.

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Related Devices (Code: JXC)

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.

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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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