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FDA 510(k)

CEFOTETAN 30 MCG ANTIMICROBIAL SUSCEPTIBILITY DISK

K-Number: K860895 · 1986-04-11

ApplicantOrganon Teknika Corp.
Decision Date1986-04-11
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CEFOTETAN 30 MCG ANTIMICROBIAL SUSCEPTIBILITY DISK is the device name listed in this FDA 510(k) record. The listed applicant is Organon Teknika Corp.. It received FDA 510(k) clearance on 1986-04-11 under 510(k) number K860895. 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 CEFOTETAN 30 MCG ANTIMICROBIAL SUSCEPTIBILITY DISK?

CEFOTETAN 30 MCG ANTIMICROBIAL SUSCEPTIBILITY DISK is a medical device that received FDA 510(k) clearance on 1986-04-11. The listed applicant is Organon Teknika Corp.. The 510(k) number is K860895.

When did CEFOTETAN 30 MCG ANTIMICROBIAL SUSCEPTIBILITY DISK receive FDA 510(k) clearance?

CEFOTETAN 30 MCG ANTIMICROBIAL SUSCEPTIBILITY DISK received FDA 510(k) clearance on 1986-04-11, under 510(k) number K860895.

Who is the listed applicant for CEFOTETAN 30 MCG ANTIMICROBIAL SUSCEPTIBILITY DISK?

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

What is the FDA product code for CEFOTETAN 30 MCG ANTIMICROBIAL SUSCEPTIBILITY DISK?

The FDA product code for CEFOTETAN 30 MCG ANTIMICROBIAL SUSCEPTIBILITY DISK 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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