ROCHE DIAGNOSTICS CK-MB
FDA 510(k) clearance K003158 · decided 2000-12-18
Clearance details
- K-number
- K003158
- Device name
- ROCHE DIAGNOSTICS CK-MB
- Applicant
- Roche Diagnostics Corp.
- Decision
- Substantially Equivalent
- Date received
- 2000-10-10
- Decision date
- 2000-12-18
- Days to decision
- 69 days
- Clearance type
- Traditional
- Product code
- JHW
- Device class
- 2
- Regulation number
- 862.1215
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Indianapolis, IN, US
- Third-party review
- No
- Expedited review
- No
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| Record | Firm | Date |
|---|---|---|
| Creatine Kinase-MB (K162526) | Roche Diagnostics | 2017-05-26 |
| ELITECH CLINICAL SYSTEMS ENVOY 500 CK REAGENT KIT (K141265) | Elitechgroup | 2014-07-18 |
| ELITECH CLINICAL SYSTEMS CK NAC SL (K122083) | Elitechgroup | 2012-08-22 |
| WIENER LAB. CK-MB DS UV UNITEST, MODEL 28 X 2.5 ML CAT. NR. 1271354 (K023744) | Wiener Laboratories Saic | 2003-01-03 |
| ELECSYS CK-MB (K961501) | Boehringer Mannheim Corp. | 1996-06-11 |
| CK-MB METHOD FOR THE TECHNICON IMMUNO 1(R) SYSTEM IN-VITRO DIAGNOSTIC SYSTEM (K950186) | Miles, Inc. | 1995-03-13 |
| LIFESIGN, CARE POINT, VITALSIGN, ACCUSIGN (K944325) | Princeton BioMeditech Corp. | 1995-02-22 |
| CREATINE KINASE MB DETERMINATION (UV) (K942958) | Biochemical Trade, Inc. | 1994-11-21 |
| AXSYM CK-MB (K935924) | Abbott Laboratories | 1994-06-21 |
| CARDIO REP CK ISOENZYME KIT - 3310 (K931050) | Helena Laboratories | 1993-04-20 |
| STAMBI-CK (K913349) | Intl. Immunoassay Laboratories, Inc. | 1991-10-23 |
| PROPOSED NEW USE OF INSTRUMENT SYSTEM AND TEST KIT (K912231) | Intl. Immunoassay Laboratories, Inc. | 1991-07-08 |
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
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|---|---|---|
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