Creative Laboratory Products, Inc.
Indianapolis, IN, US
Creative Laboratory Products, Inc. appears in FDA device records in Indianapolis, IN. FDA records list 27 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 27
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 27 510(k) clearances for Creative Laboratory Products, Inc. between 1988 and 1995. The busiest year on record is 1991, with 8. The most recent is 1995, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 7 |
| 1989 | 3 |
| 1990 | 6 |
| 1991 | 8 |
| 1992 | 1 |
| 1994 | 1 |
| 1995 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K950589 | CLP HIGH LEVEL HIGH DENSITY LIPO PROTEIN CHOLESTEROL CONTROL-HL | JJX | Substantially Equivalent | |
| K942284 | CLP TOTAL IRON AND UIBC/TIBC LINEARITY CONTROL SET | JJX | Substantially Equivalent | |
| K922995 | LIPID CONTROLS | JJX | Substantially Equivalent | |
| K913427 | SICKLE HEMOGLOBIN (HBA/S) CONTROL SET | JCM | Substantially Equivalent | |
| K913371 | TOTAL IRON AND UNSAT IRON BIND CAPAC/IRON BIND CAL | JIT | Substantially Equivalent | |
| K913585 | LIPASE LINEARITY CONTROL | JJX | Substantially Equivalent | |
| K913224 | LIPID LINEARITY CONTROLS | JJY | Substantially Equivalent | |
| K913496 | CHOLINESTERASE LINEARITY CONTROL | JJX | Substantially Equivalent | |
| K912823 | HIGH DENSITY LIPOPROTEIN CHOLESTEROL | LBR | Substantially Equivalent | |
| K912725 | TOTAL IRON & UNSAT IRON BIND CAP/IRON BIND CONTROL | JJY | Substantially Equivalent | |
| K904989 | CLP LOW LEVEL HDL CHOLESTEROL-LIPID CONTROL-II | JJY | Substantially Equivalent | |
| K902909 | CLP LOW LEVEL HDL CHOLESTEROL -LIPID CONTROL | JJY | Substantially Equivalent | |
| K896465 | CLP CK/LD ISOENZYME/IMMUNO CONTROL | JJT | Substantially Equivalent | |
| K895858 | CLP ELEVATED LIPID CONTROL | LYY | Substantially Equivalent | |
| K895862 | CLP NORMAL LIPID CONTROL | JJY | Substantially Equivalent | |
| K896247 | CLP COMPREHENSIVE LIPID CONTROL-HR | JJY | Substantially Equivalent | |
| K896246 | CLP COMPREHENSIVE LIPID CONTROL-LR | JJY | Substantially Equivalent | |
| K896335 | CLP GLYCOSYLATED HEMOGLOBIN CONTROL-NR | LCP | Substantially Equivalent | |
| K896334 | CLP GLYCOSYLATED HEMOGLOBIN CONTROL-ER | LCP | Substantially Equivalent | |
| K894554 | CLP CK/LD ISOENZYME CONTROL | JJT | Substantially Equivalent | |
| K881113 | CLP LIPOPROTEIN ELECTROPHORESIS CONTROL | JJY | Substantially Equivalent | |
| K881510 | CLP ABNORMAL COAGULATION CONTROL | GGC | Substantially Equivalent | |
| K880712 | CLP NORMAL COAGULATION CONTROL | GIZ | Substantially Equivalent | |
| K881068 | CLP ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST | GFO | Substantially Equivalent | |
| K880566 | CLP PROTHROMBIN TIME TEST | GJS | Substantially Equivalent | |
| K880713 | CLP 0.1 M SODIUM CITRATE SOLUTION | JPA | Substantially Equivalent | |
| K880711 | CLP 0.02 M CALCIUM CHLORIDE SOLUTION. | GIT | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- GFOActivated Partial Thromboplastin
- LCPAssay, Glycosylated Hemoglobin
- JITCalibrator, Secondary
- JCMControl, Hemoglobin, Abnormal
- GGCControl, Plasma, Abnormal
- JJTEnzyme Controls (Assayed And Unassayed)
- LYYLatex Patient Examination Glove
- LBRLdl & Vldl Precipitation, Hdl
- JJYMulti-Analyte Controls, All Kinds (Assayed)
- GIZPlasma, Control, Normal
- GITReagent & Control, Partial Thromboplastin Time
- JJXSingle (Specified) Analyte Controls (Assayed And Unassayed)
- JPASystem, Multipurpose For In Vitro Coagulation Studies
- GJSTest, Time, Prothrombin
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
