FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SUCROSEP THYROID STIMULATING HORMONE
K Number: K842593
·
Decision Sep 12, 1984
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
20
Review Days
71
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
- SUCROSEP THYROID STIMULATING HORMONE
- K Number
- K842593
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1690
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Boots-Celltech Diagnostics, Inc.
- Date Received
- July 3, 1984
- Decision Date
- September 12, 1984
- 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 Boots-Celltech Diagnostics, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K871877 | IDEIA HERPES SIMPLEX VIRUS TEST | Nov 17, 1989 | Substantially Equivalent |
| K880799 | MODIFIED IDEIA CHLAMYDIA TEST | Dec 8, 1988 | Substantially Equivalent |
| K880758 | SUCROSEP SPECIFIC IMMUNORADIOMETRIC ASSAY | Apr 18, 1988 | Substantially Equivalent |
| K874875 | CHEMELIA FREE THYROXINE(FT4)/ENZYME IMMUNO. (EIA) | Mar 24, 1988 | Substantially Equivalent |
| K872958 | IMAGEN INFLUENZA VIRUS A AND B TESTMI | Feb 24, 1988 | Substantially Equivalent |
| K872843 | OVEIA (TM) DUAL ANALYTE | Feb 2, 1988 | Substantially Equivalent |
| K873625 | CHEMELIA ENZYME IMMUNOASSAY FOR (TSH) | Oct 20, 1987 | Substantially Equivalent |
| K872056 | MODIFIED (DIRECTIONS FOR USE) FOR IDEIA(TM) TEST | Jun 15, 1987 | Substantially Equivalent |
| K870602 | IMAGEN HERPES SIMPLEX VIRUS (HSV) TYPING TEST | May 8, 1987 | Substantially Equivalent |
| K864998 | IDEIA(TM) CHLAMYDIA SPECIMEN COLLECTION KIT | Apr 20, 1987 | Substantially Equivalent |