FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PIPETTES, PLASTIC DISPOSABLE
K Number: K781891
·
Decision Nov 15, 1978
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
3
Applicant Total
1
Review Days
7
Basic Information
- Device Name
- PIPETTES, PLASTIC DISPOSABLE
- K Number
- K781891
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 864.6160
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- HILLWOOD CORP.
- Date Received
- November 8, 1978
- Decision Date
- November 15, 1978
- Product Code
- GJG
- 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 |
|---|---|---|---|
| GJG | Pipette, Quantitative, Hematology | FDA class 1 | Hematology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (GJG), ordered by most recent decision date.
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