FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
HCG CONTROL
K Number: K921206
·
Decision Apr 29, 1992
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
19
Review Days
47
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Basic Information
- Device Name
- HCG CONTROL
- K Number
- K921206
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Polymedco, Inc.
- Date Received
- March 13, 1992
- Decision Date
- April 29, 1992
- Product Code
- JJX
- 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 |
|---|---|---|---|
| JJX | Single (Specified) Analyte Controls (Assayed And Unassayed) | FDA class 1 | Clinical Chemistry |
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| K090703 | POLY-CHEM 90 GLUCOSE | Oct 20, 2009 | Substantially Equivalent |
| K061944 | POLY-CHEM CREATININE | Nov 3, 2006 | Substantially Equivalent |
| K053553 | NYCOCARD U-ALBUMIN AND U-ALBUMIN CONTROL | Mar 9, 2006 | Substantially Equivalent |
| K041408 | POLYMEDCO OC AUTO MICRO 80 FOB TEST | Oct 21, 2004 | Substantially Equivalent |
| K041297 | POLYMEDCO OC LIGHT FOBT TEST | Aug 12, 2004 | Substantially Equivalent |
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