Atlas FDA

ProParaFlu+ Assay

FDA 510(k) clearance K153223 · decided 2015-12-09

Clearance details

K-number
K153223
Device name
ProParaFlu+ Assay
Applicant
Hologic, Inc.
Decision
Substantially Equivalent
Date received
2015-11-06
Decision date
2015-12-09
Days to decision
33 days
Clearance type
Special
Product code
OOU
Device class
2
Regulation number
866.3980
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
San Diego, CA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Hologic

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
Panther Fusion Paraflu Assay (K172282)Hologic, Inc.2017-10-23
LYRA PARAINFLUENZA VIRUS ASSAY (K141927)Quidel Corporation2014-10-09
PROPARAFLU+ ASSAY (K132238)Gen-Probe Prodesse, Inc.2013-08-26
PROPARAFLU+ASSAY (K091053)Prodesse, Inc.2009-11-20

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
NovaSure Model 10 RF Controller (P010013/S094)Hologic, Inc.2025-12-17
Envision Mammography Platform (P080003/S011)Hologic, Inc.2025-11-24
Aptima HBV Quant Assay Kit, 100T; Aptima HBV Quant Calibrator Kit; Aptima HBV Quant Controls Kit; Aptima HBV Quant Targe (P170025/S023)Hologic, Inc.2025-10-07
ThinPrep Processor and ThinPrep Imaging System (P950039/S041)Hologic, Inc.2025-08-27
Rapid fFN Cassette Kit for the TLiIQ System, Rapid fFN Control for the TLiIQ System (P920048/S027)Hologic, Inc.2024-12-06
TLiIQ QCette (P920048/S026)Hologic, Inc.2024-10-23
Aptima CMV Quant Assay (P210029/S002)Hologic, Inc.2024-10-23
Aptima HBV Quant Assay (P170025/S022)Hologic, Inc.2024-10-23