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FDA 510(k)

VOGUES-PROSKAUER REAGENT A & B

K-Number: K930720 · 1993-04-23

ApplicantHardy Diagnostics
Decision Date1993-04-23
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VOGUES-PROSKAUER REAGENT A & B is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Diagnostics. It received FDA 510(k) clearance on 1993-04-23 under 510(k) number K930720. 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 VOGUES-PROSKAUER REAGENT A & B?

VOGUES-PROSKAUER REAGENT A & B is a medical device that received FDA 510(k) clearance on 1993-04-23. The listed applicant is Hardy Diagnostics. The 510(k) number is K930720.

When did VOGUES-PROSKAUER REAGENT A & B receive FDA 510(k) clearance?

VOGUES-PROSKAUER REAGENT A & B received FDA 510(k) clearance on 1993-04-23, under 510(k) number K930720.

Who is the listed applicant for VOGUES-PROSKAUER REAGENT A & B?

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

What is the FDA product code for VOGUES-PROSKAUER REAGENT A & B?

The FDA product code for VOGUES-PROSKAUER REAGENT A & B is JTO.

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Related Devices (Code: JTO)

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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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