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FDA 510(k)

NETILMICIN 30 MCG SENSI DISC

K-Number: K830732 · 1983-04-08

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1983-04-08
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

NETILMICIN 30 MCG 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 1983-04-08 under 510(k) number K830732. 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 NETILMICIN 30 MCG SENSI DISC?

NETILMICIN 30 MCG SENSI DISC is a medical device that received FDA 510(k) clearance on 1983-04-08. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K830732.

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

NETILMICIN 30 MCG SENSI DISC received FDA 510(k) clearance on 1983-04-08, under 510(k) number K830732.

Who is the listed applicant for NETILMICIN 30 MCG 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 NETILMICIN 30 MCG SENSI DISC?

The FDA product code for NETILMICIN 30 MCG 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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