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FDA 510(k)

TICARCILLIN SYSCEPT. DISKS

K-Number: K822394 · 1982-09-21

ApplicantBeecham Laboratories
Decision Date1982-09-21
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TICARCILLIN SYSCEPT. DISKS is the device name listed in this FDA 510(k) record. The listed applicant is Beecham Laboratories. It received FDA 510(k) clearance on 1982-09-21 under 510(k) number K822394. 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 SYSCEPT. DISKS?

TICARCILLIN SYSCEPT. DISKS is a medical device that received FDA 510(k) clearance on 1982-09-21. The listed applicant is Beecham Laboratories. The 510(k) number is K822394.

When did TICARCILLIN SYSCEPT. DISKS receive FDA 510(k) clearance?

TICARCILLIN SYSCEPT. DISKS received FDA 510(k) clearance on 1982-09-21, under 510(k) number K822394.

Who is the listed applicant for TICARCILLIN SYSCEPT. DISKS?

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

What is the FDA product code for TICARCILLIN SYSCEPT. DISKS?

The FDA product code for TICARCILLIN SYSCEPT. DISKS is JTN.

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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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