Dispens-O-Disc Meropenem

FDA 510(k) K963508 · Difco Laboratories, Inc.

Substantially Equivalent

510(k) numberK963508

Submission

Device name
Dispens-O-Disc Meropenem
Applicant
Difco Laboratories, Inc.
Livouia, MI, US
Received
September 3, 1996
Decision date
September 26, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JTN – Susceptibility Test Discs, Antimicrobial
Device class
Class II (moderate risk)
Regulation
21 CFR 866.1620
Specialty
Microbiology

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K253105HardyDisk AST Cefiderocol 30µg (FDC30)JTN · Traditional Hardy Diagnostics11/20/2025SE
K251879Sulopenem SPM 2 µgJTN · Traditional Liofilchem08/12/2025SE
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More from Thermo Fisher Scientific (Oxoid Ltd.)

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K971211Dispens-O-Disc SparfloxacinJTN · Traditional 04/14/1997SE
K971120Dispens-O-Disc (TM) LevofloxacinJTN · Traditional 04/14/1997SE
K961148Cefepime Dispans-O-Disc (Cefeplime - 30MCG)JTW · Traditional 04/26/1996SE
K954783Dryslide CartarrhalisJTO · Traditional 02/06/1996SE
K954784Dryside NeisseriaLTS · Traditional 01/30/1996SE
K953129Esp Culture System - MycoMDB · Traditional 12/26/1995SE
K950706Dryslide CoagulaseJTL · Traditional 05/16/1995SE
K944275Dispens-O-Disc Piperacillin 100 Mcg./Tazobactam 10 Mcg.JTN · Traditional 12/19/1994SE
K941016Dispens-O-Disc(Tm) NitrocefinJTO · Traditional 06/30/1994SE
K934894Cultureswab Transport SystemJTW · Traditional 02/22/1994SE

Questions and answers

When was Dispens-O-Disc Meropenem cleared by the FDA?

Dispens-O-Disc Meropenem (K963508) received a 510(k) decision of Substantially Equivalent on September 26, 1996, 23 days after the submission was received.

What is the product code of K963508?

The FDA product code is JTN – Susceptibility Test Discs, Antimicrobial, a Class II (moderate risk) device regulated under 21 CFR 866.1620.