Atlas FDA

HARDYCHROM MRSA

FDA 510(k) clearance K102922 · decided 2011-05-04

Clearance details

K-number
K102922
Device name
HARDYCHROM MRSA
Applicant
Hardy Diagnostics
Decision
Substantially Equivalent
Date received
2010-10-01
Decision date
2011-05-04
Days to decision
215 days
Clearance type
Traditional
Product code
JSO
Device class
2
Regulation number
866.1700
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Santa Maria, CA, 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
HardyCHROM CRE (K190553)Hardy Diagnostics2019-04-29
CHROMID CARBA agar (CARB) (K181092)Biomerieux S.A.2018-07-06
MRSASelect II (K171061)Bio-Rad2017-12-28
Remel Spectra ESBL (K162620)Remel, Inc.2017-05-01
HardyCHROM ESBL (K160512)Hardy Diagnostics2016-11-15
chromID MRSA (K162076)bioMerieux, Inc.2016-10-25
chromID MRSA (K151688)bioMerieux, Inc.2016-03-11
VRESELECT CULTURE MEDIUM (K122187)Bio-Rad2012-11-06
VRESELECT CULTURE MEDIUM (K103684)Bio-Rad2011-10-21
MRSA SELECT - SKIN AND SOFT TISSUE WOUND SPECIMENS (K100589)Bio-Rad2010-10-29
REMEL SPECTRA MRSA (K092407)Remel, Inc.2010-10-08
BBL CHROMAGAR MRSA II (K092767)Becton, Dickinson & CO2010-08-20

Recalls involving this device

RecordFirmDate
HardyCHROM MRSA,REF; G307, LOT: 447694, A selective and differential chromogenic medium fo recall (Z-2298-2020)Hardy Diagnostics2020-06-09
HardyCHROM MRSA Cat no: G307 Lot no: H15155 Expires: 2015-08-13 Container Type: 15x100mm m recall (Z-2463-2015)Hardy Diagnostics2015-08-26