Atlas FDA

KALLESTAD RSV MICROPLATE EIA

FDA 510(k) clearance K924289 · decided 1993-02-12

Clearance details

K-number
K924289
Device name
KALLESTAD RSV MICROPLATE EIA
Applicant
Bio-Rad Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1992-08-21
Decision date
1993-02-12
Days to decision
175 days
Clearance type
Traditional
Product code
MCE
Device class
1
Regulation number
866.3480
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Chaska, MN, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
QUICKVUE RSV (20 TEST KIT), MODEL 20193; (2 TEST KIT), MODEL 20199 (K061008)Quidel Corp.2006-09-08

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
MONOLISA ANTI-HBC IGM EIA (P060034/S008)Bio-Rad Laboratories, Inc.2014-03-19
BIO-RAD MONOLISA ANTI-HBC IGM EIA (P060034/S007)Bio-Rad Laboratories, Inc.2013-12-12
BIO-RAD MONOLISA ANTI-HBC EIA (P060031/S007)Bio-Rad Laboratories, Inc.2013-12-12
BIO-RAD MONOLISA ANTI-HBC EIA (P060031/S006)Bio-Rad Laboratories, Inc.2012-11-13
BIO-RAD MONOLISA ANTI-HBC IGM EIA (P060034/S006)Bio-Rad Laboratories, Inc.2012-11-13
BIO-RAD MONOLISA ANTI-HBC EIA (P060031/S005)Bio-Rad Laboratories, Inc.2011-04-28
BIO-RAD MONOLISA ANTI-HBC EIA (P060031/S003)Bio-Rad Laboratories, Inc.2010-12-30
MONOLISA ANTI-HBC IGM EIA (P060034/S005)Bio-Rad Laboratories, Inc.2010-11-23