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FDA 510(k)

V FACTOR DISCS

K-Number: K802501 · 1980-11-12

ApplicantOxoid U.S.A., Inc.
Decision Date1980-11-12
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

V FACTOR DISCS 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 1980-11-12 under 510(k) number K802501. 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 V FACTOR DISCS?

V FACTOR DISCS is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K802501.

When did V FACTOR DISCS receive FDA 510(k) clearance?

V FACTOR DISCS received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802501.

Who is the listed applicant for V FACTOR DISCS?

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 V FACTOR DISCS?

The FDA product code for V FACTOR DISCS 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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