Atlas FDA

PLATELIA TOXO IGM KIT MODEL 26211

FDA 510(k) clearance K090847 · decided 2009-07-01

Clearance details

K-number
K090847
Device name
PLATELIA TOXO IGM KIT MODEL 26211
Applicant
Bio-Rad Laboratories
Decision
Substantially Equivalent
Date received
2009-03-30
Decision date
2009-07-01
Days to decision
93 days
Clearance type
Special
Product code
LGD
Device class
2
Regulation number
866.3780
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Redmond, WA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Platelia Toxo IgM assa recall (Z-2515-2025)Bio-Rad Laboratories, Inc.2025-09-04

PMA approvals by this applicant

RecordFirmDate
MONOLISA ANTI-HBS EIA (P050048/S010)Bio-Rad Laboratories2025-04-18
BIO-RAD MONOLISA ANTI-HBS EIA (P050048/S009)Bio-Rad Laboratories2013-12-12
BIO-RAD MONOLISA ANTI-HBS EIA (P050048/S008)Bio-Rad Laboratories2012-11-13
BIO-RAD MONOLISA ANTI-HBS EIA AND MONOLISA ANTI-HBS CALIBRATOR KIT (P050048/S007)Bio-Rad Laboratories2012-11-13
BIO-RAD MONOLISA ANTI-HBS EIA (P050048/S004)Bio-Rad Laboratories2011-04-25
MONOLISA ANTI-HBS EIA AND MONOLISA ANTI-HBS CALIBRATOR KIT (P050048/S005)Bio-Rad Laboratories2010-11-23
BIO-RAD MONOLISA ANTI -HBS EIA (P050048/S006)Bio-Rad Laboratories2010-09-27
BIO-RAD MONOLISA ANTI-HBS EIA (P050048/S002)Bio-Rad Laboratories2010-03-12