FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BLOOD GAS CONTROL PROD. NO. BG-1, BG-2
K Number: K801449
·
Decision Jul 21, 1980
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
66
Applicant Total
2
Review Days
28
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Basic Information
- Device Name
- BLOOD GAS CONTROL PROD. NO. BG-1, BG-2
- K Number
- K801449
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Health Diagnostics Corp.
- Date Received
- June 23, 1980
- Decision Date
- July 21, 1980
- Product Code
- JJS
- 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 |
|---|---|---|---|
| JJS | Controls For Blood-Gases, (Assayed And Unassayed) | FDA class 1 | Clinical Chemistry |
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Other Clearances by Health Diagnostics Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K802334 | IN-HOME EARLY PREGNANCY TEST KIT | Oct 10, 1980 | Substantially Equivalent |