Atlas FDA

HEPARIN LOCK / FLUSH SYRINGES

FDA 510(k) clearance K133446 · decided 2014-11-14

Clearance details

K-number
K133446
Device name
HEPARIN LOCK / FLUSH SYRINGES
Applicant
Excelsior Medical Corporation
Decision
Substantially Equivalent
Date received
2013-11-12
Decision date
2014-11-14
Days to decision
367 days
Clearance type
Traditional
Product code
NZW
Device class
2
Regulation number
880.5200
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Neptune, NJ, 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
BD PosiFlush Heparin Lock Flush Syringe (K163591)Becton, Dickinson and Company2017-02-27
HEPARIN LOCK FLUSH SOLUTION USP, MODELS 504401, 504411, 504505, 505701, 504901, 1710 (K092938)App Pharmaceuticals, LLC2010-06-18
MEDEFIL'S HEPARIN I.V. FLUSH SYRINGE 1 UNIT/ML; 10 UNITS/ML; AND 100 UNITS/ML IN VARIOUS FILL SIZES (K092491)Medefil, Inc.2010-02-03
HEPARIN LOCK FLUSH SOLUTION, USP BD POSIFLUSH HEPARIN LOCK FLUSH SYRINGE (K090680)Becton, Dickinson & CO2009-06-10
SYREX HEPARIN LOCK FLUSH SYRINGE, 1 UNIT/ML & 2 UNITS/ML (K061497)Excelsior Medical Corp.2007-02-23
SYREX PRE-FILLED SYRINGE (K023740)Excelsior Medical Corp.2003-05-13

Recalls involving this device

RecordFirmDate
Excelsior Heparin Sodium, Porcine, Preservative Free 100 U / mL Solution Prefilled Syringe recall (Z-1596-2022)Mckesson Medical-Surgical Inc. Corporate Office2022-08-26