LYFO(TM) DIFFERENTIAL DISK— 510(k) K945487

Name: FDA 510(k) clearance K945487
Creator: U.S. Food and Drug Administration
Published: 1995-05-11

Substantially Equivalent

Microbiologics, Inc.

FDA 510(k) clearance K945487 for LYFO(TM) DIFFERENTIAL DISK, Substantially Equivalent on 1995-05-11. Applicant: Microbiologics, Inc.. Device class: 1.

Clearance details

Applicant: Microbiologics, Inc.
Product code: Code JSP
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1994-11-08
Decision date: 1995-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Cloud, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JSP

view all

K945488 — LYFO(TM) DIFFERENTIAL DISK1995-05-11
K945489 — LYFO(TM) DIFFERENTIAL DISK1995-05-11
K944528 — BBLCRYSTAL ANAEROBE ID SYSTEM1995-03-07
K910666 — VITEK ANAEROBE IDENTIFICATION CARD, MODIFICATION1991-04-03
K900996 — VITEK ANAEROBE IDENTIFICATION CARD1990-05-11

More clearances from Microbiologics, Inc.

view all

K190086 — Cepheid Xpert Respiratory Control Panel2019-10-07
K191168 — Cepheid Xpert SA Nasal Complete Control Panel2019-06-25
K191172 — Cepheid Xpert MRSA NxG Control Panel2019-06-20
K190223 — Cepheid Xpert CT/NG Control Panel2019-05-08
K190463 — Cepheid Xpert C. difficile/Epi Control Panel2019-04-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.