DIMENSION(R) LACTIC ACID METHOD
FDA 510(k) clearance K914508 · decided 1991-11-27
Clearance details
- K-number
- K914508
- Device name
- DIMENSION(R) LACTIC ACID METHOD
- Applicant
- E.I. Dupont DE Nemours & Co., Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-10-09
- Decision date
- 1991-11-27
- Days to decision
- 49 days
- Clearance type
- Traditional
- Product code
- KHP
- Device class
- 1
- Regulation number
- 862.1450
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Wilmington, DE, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch E.I. Dupont DE Nemours & Co.
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.
| Record | Firm | Date |
|---|---|---|
| PICCOLO LACTATE TEST SYSTEM (K130113) | Abaxis, Inc. | 2013-03-11 |
| RAPIDPOINT 500 BLOOD GAS ANALYER (K113216) | Siemens Healthcare Diagnostics | 2012-05-03 |
| NOVA STATSTRIP LACTATE HOSPITAL METER SYSTEM (K112955) | Nova Biomedical Corporation | 2012-01-05 |
| 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 |
| LACTATE PRO SYSTEM (K980908) | Kdk Corp. | 1998-09-11 |
| 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 |
Recalls involving this device
No recalls on record reference this clearance.