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FDA 510(k)

TICARCILLIN/CLVULINIC ACID 85 MCG SUSCEPTIBILITY D

K-Number: K871674 · 1987-05-15

Decision Date1987-05-15
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TICARCILLIN/CLVULINIC ACID 85 MCG SUSCEPTIBILITY D 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 1987-05-15 under 510(k) number K871674. 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 TICARCILLIN/CLVULINIC ACID 85 MCG SUSCEPTIBILITY D?

TICARCILLIN/CLVULINIC ACID 85 MCG SUSCEPTIBILITY D is a medical device that received FDA 510(k) clearance on 1987-05-15. The listed applicant is Organon Teknika Corp.. The 510(k) number is K871674.

When did TICARCILLIN/CLVULINIC ACID 85 MCG SUSCEPTIBILITY D receive FDA 510(k) clearance?

TICARCILLIN/CLVULINIC ACID 85 MCG SUSCEPTIBILITY D received FDA 510(k) clearance on 1987-05-15, under 510(k) number K871674.

Who is the listed applicant for TICARCILLIN/CLVULINIC ACID 85 MCG SUSCEPTIBILITY D?

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 TICARCILLIN/CLVULINIC ACID 85 MCG SUSCEPTIBILITY D?

The FDA product code for TICARCILLIN/CLVULINIC ACID 85 MCG SUSCEPTIBILITY D is JTN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Organon Teknika Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 130 devices →

Related Devices (Code: JTN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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