FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BHCG RIA KIT
K Number: K831264
·
Decision Jun 8, 1983
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
42
Review Days
51
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Basic Information
- Device Name
- BHCG RIA KIT
- K Number
- K831264
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1155
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Micromedic Systems
- Date Received
- April 18, 1983
- Decision Date
- June 8, 1983
- 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 |
Similar 510(k) Clearances
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Other Clearances by Micromedic Systems
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|---|---|---|---|
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| K871008 | MICROMEDIC NEONATAL T4 KIT | May 26, 1987 | Substantially Equivalent |
| K870904 | MICROMEDIC NEONATAL TSH MONOCLONAL IRMA KIT | May 26, 1987 | Substantially Equivalent |
| K870245 | AUTOPAK TSH MONOCLONAL IRMA KIT | Apr 1, 1987 | Substantially Equivalent |
| K862206 | TAURUS (TM) AUTOMATIC LIQUID SCINTILLATION COUNTER | Aug 4, 1986 | Substantially Equivalent |
| K860813 | MICROMEDIC HTSH MONOCLONAL IRMA KIT | Jul 14, 1986 | Substantially Equivalent |
| K861262 | MMS T3 UPTAKE | May 23, 1986 | Substantially Equivalent |
| K861320 | MMS T4 RIA KIT | Apr 24, 1986 | Substantially Equivalent |