LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110— 510(k) K862848

Name: FDA 510(k) clearance K862848
Creator: U.S. Food and Drug Administration
Published: 1986-12-18

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K862848 for LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110, Substantially Equivalent on 1986-12-18. Applicant: Lkb Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Lkb Instruments, Inc.
Product code: Code GWC
Device class: Class 1
Regulation: 21 CFR 866.3740
Advisory panel: Microbiology
Date received: 1986-07-29
Decision date: 1986-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gaithersburg, MD, US

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