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FDA 510(k)

THYMINE/THYMIDINE DISCS DDG

K-Number: K830939 · 1983-04-13

ApplicantOxoid U.S.A., Inc.
Decision Date1983-04-13
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

THYMINE/THYMIDINE DISCS DDG is the device name listed in this FDA 510(k) record. The listed applicant is Oxoid U.S.A., Inc.. It received FDA 510(k) clearance on 1983-04-13 under 510(k) number K830939. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THYMINE/THYMIDINE DISCS DDG?

THYMINE/THYMIDINE DISCS DDG is a medical device that received FDA 510(k) clearance on 1983-04-13. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K830939.

When did THYMINE/THYMIDINE DISCS DDG receive FDA 510(k) clearance?

THYMINE/THYMIDINE DISCS DDG received FDA 510(k) clearance on 1983-04-13, under 510(k) number K830939.

Who is the listed applicant for THYMINE/THYMIDINE DISCS DDG?

The FDA 510(k) record lists Oxoid U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THYMINE/THYMIDINE DISCS DDG?

The FDA product code for THYMINE/THYMIDINE DISCS DDG is JTO.

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Other records listing Oxoid U.S.A., Inc. as applicant

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Related Devices (Code: JTO)

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K050352IN-VITRO DIAGNOSTIC VAGINITIS TEST KITAmeritek Research, LLCK970832PYR SWABRemel, Inc.K970834GRAM SWABRemel, Inc.K970833INDOLE SWABRemel, Inc.K970009LYFO(TM) DIFFERENTIAL DISK-BACITRACINMicrobiologics, Inc.K962966IDS RAPID CB PLUS SYSTEMInnovative Diagnostic Systems, Inc.

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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