FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BLANKING SOLUTION HGB
K Number: K771789
·
Decision Oct 7, 1977
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
38
Applicant Total
54
Review Days
17
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Basic Information
- Device Name
- BLANKING SOLUTION HGB
- K Number
- K771789
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.5620
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- J.T. Baker Chemical Co.
- Date Received
- September 20, 1977
- Decision Date
- October 7, 1977
- Product Code
- GKR
- Advisory Committee
- Hematology
- Review Advisory Committee
- HE
- 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 |
|---|---|---|---|
| GKR | System, Hemoglobin, Automated | FDA class 2 | Hematology |
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Other Clearances by J.T. Baker Chemical Co.
| K Number | Device Name | ||
|---|---|---|---|
| K803128 | SERIES 810 PLATELET ANALYZER | Apr 3, 1981 | Substantially Equivalent |
| K802080 | BAKER DIAG. ULTRARATE CHLORIDE KIT | Oct 10, 1980 | Substantially Equivalent |
| K802035 | BAKER DIAG. ULTRARATE CO2 REAGENT KIT | Sep 26, 1980 | Substantially Equivalent |
| K801909 | LSA 290 ASSAY REAGENTS/NEPHELOMETRIC | Sep 26, 1980 | Substantially Equivalent |
| K801662 | J.T. BAKER ALPHA-2-MACROGLOBULIN NEPH. | Sep 16, 1980 | Substantially Equivalent |
| K801669 | J.T. BAKER ALPHA-1-ANTITRYPSIN NEPHELO | Sep 16, 1980 | Substantially Equivalent |
| K801661 | J.T. BAKER CERULOPLASMIN NEPHELOMETRIC | Sep 16, 1980 | Substantially Equivalent |
| K801795 | BAKER DIAGNOSTIC ULTRA-RATE SODIUM/POT. | Sep 16, 1980 | Substantially Equivalent |
| K801362 | ALBUMIN NEPHELOMETRIC ASSAY | Jul 21, 1980 | Substantially Equivalent |
| K801432 | HEMOPEXIN NEPHELOMETRIC ASSAY | Jul 8, 1980 | Substantially Equivalent |