FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CONTRAST STRIP HCG
K Number: K964156
·
Decision Nov 25, 1996
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
5
Review Days
40
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Basic Information
- Device Name
- CONTRAST STRIP HCG
- K Number
- K964156
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1155
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Genzyme Diagnostics
- Date Received
- October 16, 1996
- Decision Date
- November 25, 1996
- Product Code
- JHI
- 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 |
|---|---|---|---|
| JHI | Visual, Pregnancy Hcg, Prescription Use | FDA class 2 | Clinical Chemistry |
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Other Clearances by Genzyme Diagnostics
| K Number | Device Name | ||
|---|---|---|---|
| K043385 | OSOM HCG COMBO TEST | Apr 12, 2005 | Substantially Equivalent |
| K983399 | GIARDIA/CRYPTOSPORIDIUM COMBO RAPID ASSAY | Jan 11, 1999 | Substantially Equivalent |
| K963425 | GENZYME DIAGNOSTICS CONTRAST MONO | Feb 25, 1997 | Substantially Equivalent |
| K964155 | CONTRAST HCG URINE/SERUM TEST AND RAPID HCG URINE/SERUM TEST | Nov 25, 1996 | Substantially Equivalent |