Atlas FDA

LACTATE PRO SYSTEM

FDA 510(k) clearance K980908 · decided 1998-09-11

Clearance details

K-number
K980908
Device name
LACTATE PRO SYSTEM
Applicant
Kdk Corp.
Decision
Substantially Equivalent
Date received
1998-03-10
Decision date
1998-09-11
Days to decision
185 days
Clearance type
Traditional
Product code
KHP
Device class
1
Regulation number
862.1450
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Kyoto, JP
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
PICCOLO LACTATE TEST SYSTEM (K130113)Abaxis, Inc.2013-03-11
RAPIDPOINT 500 BLOOD GAS ANALYER (K113216)Siemens Healthcare Diagnostics2012-05-03
NOVA STATSTRIP LACTATE HOSPITAL METER SYSTEM (K112955)Nova Biomedical Corporation2012-01-05
I-STAT LACTATE TEST/I-SAT CG4+CARTRIDGE (K112430)Abbott Pont of Care, Inc.2011-12-20
NOVA STATSTRIP LACTATE HOSPITAL METER, NOVA STATSTRIP LACTATE TEST STRIPS (K100602)Nova Biomedical Corp.2011-08-17
EPOC BGEM, EPOC READER, EPOC HOST, EPOC CARE-FILL CAPILLARY TUBE (K093297)Epocal, Inc.2010-06-09
IRMA SL BLOOD ANALYSIS SYSTEM LACTATE CARTRIDGE (K013938)Diametrics Medical, Inc.2002-01-28
I-STAT SYSTEM (K011478)I-Stat Corp.2001-07-02
I-STAT LACTATE TEST (K982071)I-Stat Corp.1998-06-29
LACTEST I (K971944)Jwt, Inc.1997-12-17
ACCUSPORT LACTATE MONITORING SYSTEM LACTATE TEST STRIPS ACCUSPORT MONITOR (K951331)Boehringer Mannheim Corp.1995-08-11
STAT PROFILE PLUS 9 ANALYZER (K936066)Nova Biomedical Corp.1995-03-09

Recalls involving this device

No recalls on record reference this clearance.