FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
FIAGEN(TM) HTSH CATALOGUE NUMBER: 101-301
K Number: K874622
·
Decision Dec 18, 1987
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
17
Review Days
38
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
- FIAGEN(TM) HTSH CATALOGUE NUMBER: 101-301
- K Number
- K874622
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1690
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Cyberfluor, Inc.
- Date Received
- November 10, 1987
- Decision Date
- December 18, 1987
- 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 Cyberfluor, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K923410 | FIAGEN PROGESTERONE | Dec 3, 1992 | Substantially Equivalent |
| K905656 | FLAGEN TRIIODOTHYRONINE (T3) ASSAY | Jan 23, 1991 | Substantially Equivalent |
| K904539 | FLAGEN TM FREE T4 | Nov 30, 1990 | Substantially Equivalent |
| K900621 | FIAGEN(TM) HLH.S | Mar 1, 1990 | Substantially Equivalent |
| K895186 | FIAGEN T3 UPTAKE CATALOGUE #101-402 | Nov 8, 1989 | Substantially Equivalent |
| K895396 | CYBERFLUOR FIAGEN TSH | Oct 31, 1989 | Substantially Equivalent |
| K884708 | FIAGEN HFSH TIME-RESOLVED FLUOROIMMUNOASSAY KIT | Jan 17, 1989 | Substantially Equivalent |
| K884707 | FIAGEN DIGOXIN TIME-RESOLVED FLUOROIMMUNOASSAY KIT | Jan 17, 1989 | Substantially Equivalent |
| K884201 | FIAGEN TBG TIME-RESOLVED FLUOROIMMUNOASSAY KIT | Dec 14, 1988 | Substantially Equivalent |
| K883182 | FIAGEN RUBELLA IGG | Oct 31, 1988 | Substantially Equivalent |