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FDA 510(k)

MINOCYCLINE 30MCG. SENSI DISC

K-Number: K802194 · 1980-10-23

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1980-10-23
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MINOCYCLINE 30MCG. SENSI DISC is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802194. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINOCYCLINE 30MCG. SENSI DISC?

MINOCYCLINE 30MCG. SENSI DISC is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K802194.

When did MINOCYCLINE 30MCG. SENSI DISC receive FDA 510(k) clearance?

MINOCYCLINE 30MCG. SENSI DISC received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802194.

Who is the listed applicant for MINOCYCLINE 30MCG. SENSI DISC?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINOCYCLINE 30MCG. SENSI DISC?

The FDA product code for MINOCYCLINE 30MCG. SENSI DISC is JTN.

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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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