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FDA 510(k)

YEAST IDENT

K-Number: K830286 · 1983-04-05

ApplicantAnalytical Products, Inc.
Decision Date1983-04-05
Product CodeJXB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

YEAST IDENT is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Products, Inc.. It received FDA 510(k) clearance on 1983-04-05 under 510(k) number K830286. The device is classified under product code JXB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YEAST IDENT?

YEAST IDENT is a medical device that received FDA 510(k) clearance on 1983-04-05. The listed applicant is Analytical Products, Inc.. The 510(k) number is K830286.

When did YEAST IDENT receive FDA 510(k) clearance?

YEAST IDENT received FDA 510(k) clearance on 1983-04-05, under 510(k) number K830286.

Who is the listed applicant for YEAST IDENT?

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

What is the FDA product code for YEAST IDENT?

The FDA product code for YEAST IDENT is JXB.

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Other records listing Analytical Products, Inc. as applicant

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Related Devices (Code: JXB)

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.

K080719YEAST TRAFFIC LIGHT PNA FISHAdvandx, Inc.K062461C. ALBICANS PNA FISHAdvandx, Inc.K993554YEASTESTDiagnostic Markers, Inc.K943621RAPID YEAST PLUS SYSTEMInnovative Diagnostic Systems, Inc.K935124BACTICARD CANDIDARemel Co.K900112MICRORING YTMedical Wire & Equipment Co.

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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