FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BIOCHECK SENSITIVE TSH (S-TSH) ENZYME IMMUNOASSAY TEST KIT; CATALOG NUMBER: BC-1003
K Number: K990993
·
Decision Jun 22, 1999
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
14
Review Days
90
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
- BIOCHECK SENSITIVE TSH (S-TSH) ENZYME IMMUNOASSAY TEST KIT; CATALOG NUMBER: BC-1003
- K Number
- K990993
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1690
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Biocheck, Inc.
- Date Received
- March 24, 1999
- Decision Date
- June 22, 1999
- Product Code
- JLW
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| JLW | Radioimmunoassay, Thyroid-Stimulating Hormone | FDA class 2 | Clinical Chemistry |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (JLW), ordered by most recent decision date.
Atellica® IM TSH3-Ultra II (TSH3ULII)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Dimension LOCI Thyroid Stimulating Hormone Flex reagent cartridge (TSHL); Dimension LOCI Free Thyroxine Flex reagent cartridge (FT4L)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Maverick Diagnostic System TC1000; Maverick Test Panel A0.B0
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ADVIA Centaur® TSH3-Ultra II (TSH3ULII)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Atellica® CI Analyzer, Atellica® IMThyroid Stimulating Hormone 3-Ultra (TSH3-UL), Atellica® CH Albumin BCP (AlbP)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Other Clearances by Biocheck, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K041619 | BIO CHECK WHOLE BLOOD/PLASMA/SERMON MODEL #801116 | Dec 17, 2004 | Substantially Equivalent |
| K040030 | BIOCHECK CARDIAC-1 CRP RAPID TEST, MODEL BC-804114 | Jun 16, 2004 | Substantially Equivalent |
| K022660 | BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117 | Dec 19, 2002 | Substantially Equivalent |
| K013062 | BIOCHECK HUMAN CARDIAC TROPONIN-I IMMUNOASSAY TEST KIT | Jan 8, 2002 | Substantially Equivalent |
| K003851 | BIOCHECK HIGH SENSITIVITY C-REACTIVE PROTEIN ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1119 | Jul 20, 2001 | Substantially Equivalent |
| K002294 | BIOCHECK TESTOSTERONE EIA, MODEL BC-1115 | Oct 2, 2000 | Substantially Equivalent |
| K001022 | BIOCHECK, INC. B-2 MICROGLOBIN ENZYME IMMUNOASAY TEST KIT, MODEL BC-1061 | Sep 26, 2000 | Substantially Equivalent |
| K992517 | BIOCHECK FERRITIN ELISA MODEL BC-1025 | Sep 24, 1999 | Substantially Equivalent |
| K992528 | BIOCHECK IGE ELISA, MODEL BC-1035 | Sep 21, 1999 | Substantially Equivalent |
| K991741 | BIOCHECK HCG ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1027 | Jul 22, 1999 | Substantially Equivalent |