FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
VIGIL TDM CONTROLS
K Number: K972819
·
Decision Aug 13, 1997
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
201
Applicant Total
281
Review Days
15
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- VIGIL TDM CONTROLS
- K Number
- K972819
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.3280
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Beckman Instruments, Inc.
- Date Received
- July 29, 1997
- Decision Date
- August 13, 1997
- Product Code
- DIF
- Advisory Committee
- Clinical Toxicology
- Review Advisory Committee
- TX
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DIF | Drug Mixture Control Materials | FDA class 1 | Clinical Toxicology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (DIF), ordered by most recent decision date.
Detectabuse Liquid Control Urine, Detectabuse Stat-Skreen Liquid Control Urine, Detectabuse Liquid Control Urine, AU/NZ, Detectabuse Liquid Control Urine, Immunoassay Series, Detectabuse Liquid Control Urine, GC/MS and Confirm series
FDA 510(k)
FDA Class 1
·Clinical Toxicology
SALIVABUSE LIQUID ORAL FLUID CONTROL, SALIVABUSE LIQUID ORAL FLUID CONTROL, AU/NZ
FDA 510(k)
FDA Class 1
·Clinical Toxicology
MULTICHEM WBT
FDA 510(k)
FDA Class 1
·Clinical Toxicology
DETECTABUSE LIQUID CONTROL, DETECTABUSE STAT-SKREEN LIQUID CONTROL
FDA 510(k)
FDA Class 1
·Clinical Toxicology
LIQUICHEK WHOLE BLOOD IMMUNOSUPPRESSANT CONTROL TILEVEL (1,2 AND 3)
FDA 510(k)
FDA Class 1
·Clinical Toxicology
LIQUICHEK URINE TOXICOLOGY CONTROL, S10 & S10 MINIPAK, LIQUICHEK URINE TOXICOLOGY CONTROL, LEVEL S20 & LEVEL S20 MINIPAK
FDA 510(k)
FDA Class 1
·Clinical Toxicology
Other Clearances by Beckman Instruments, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K973448 | ACCESS TOXOPLASMA IGM REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 34460, 34465, 34469 | Sep 17, 1998 | Substantially Equivalent |
| K982250 | ACCESS FREE T4 REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER | Jul 14, 1998 | Substantially Equivalent |
| K981403 | IMMAGE IMMUNOCHEMISTRY SYSTEM VALPROIC ACID (VPA) REAGENT | May 8, 1998 | Substantially Equivalent |
| K981354 | ACCESS AFP REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER MODEL NUMBER 33211 | May 1, 1998 | Substantially Equivalent |
| K980173 | ACCESS TOTAL BHCG REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER; 33500, 33505 | Mar 18, 1998 | Substantially Equivalent |
| K974816 | ACCESS(R) PSA REAGENTS ON THE ACCESS(R) IMMUNOASSAY ANALYZER 33220, 33225, 33229 | Feb 20, 1998 | Substantially Equivalent |
| K974564 | IMMAGE IMMUNOCHEMISTRY SYSTEM ALPHA-2-MACROGLOBULIN REAGENT | Feb 17, 1998 | Substantially Equivalent |
| K974110 | IMMAGE IMMUNOCHEMISTRY SYSTEM ANTITHROMBIN III (AT3) REAGENT | Dec 24, 1997 | Substantially Equivalent |
| K974452 | VIGIL LIPID CONTROL | Dec 17, 1997 | Substantially Equivalent |
| K973932 | BECKMAN CALIBRATOR 2 (CAL2) | Dec 15, 1997 | Substantially Equivalent |