OXOID ANTIMICROBIAL SUSCEPTIBILITY DISCS

Susceptibility Test Discs, Antimicrobial

OXOID U.S.A., INC.

The following data is part of a premarket notification filed by Oxoid U.s.a., Inc. with the FDA for Oxoid Antimicrobial Susceptibility Discs.

Pre-market Notification Details

• Device ID: K860153
• 510k Number: K860153
• Device Name: OXOID ANTIMICROBIAL SUSCEPTIBILITY DISCS
• Classification: Susceptibility Test Discs, Antimicrobial
• Applicant: OXOID U.S.A., INC. WADE RD. BASINGSTROKE Hampshire Rg 24 Op, GB
• Contact: E. Y Bridson
• Correspondent: E. Y Bridson; OXOID U.S.A., INC. WADE RD. BASINGSTROKE Hampshire Rg 24 Op, GB
• Product Code: JTN
• CFR Regulation Number: 866.1620 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1986-01-15
• Decision Date: 1986-03-04

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
05032384007066	K860153	000
05032384005895	K860153	000
05032384005888	K860153	000
05032384005833	K860153	000
05032384005819	K860153	000
05032384005789	K860153	000
05032384005765	K860153	000
05032384005758	K860153	000
05032384005710	K860153	000
05032384005697	K860153	000
05032384005659	K860153	000
05032384005635	K860153	000
05032384005628	K860153	000
05032384005581	K860153	000
05032384005567	K860153	000
05032384005550	K860153	000
05032384005536	K860153	000
05032384005529	K860153	000
05032384005925	K860153	000
05032384005970	K860153	000
05032384006656	K860153	000
05032384006649	K860153	000
05032384006564	K860153	000
05032384006502	K860153	000
05032384006472	K860153	000
05032384006410	K860153	000
05032384006403	K860153	000
05032384006373	K860153	000
05032384006342	K860153	000
05032384006304	K860153	000
05032384006298	K860153	000
05032384006281	K860153	000
05032384006205	K860153	000
05032384006090	K860153	000
05032384006038	K860153	000
05032384006014	K860153	000
05032384005994	K860153	000
05032384005505	K860153	000