510(k) K781891
- Device
- PIPETTES, PLASTIC DISPOSABLE
- Applicant
- HILLWOOD CORP.
- 510(k) number
- K781891
- Product code
- GJG
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1978-11-15
- Date received
- 1978-11-08
- Regulation
- 864.6160
- Classification name
- Pipette, Quantitative, Hematology
- Medical specialty
- Hematology
- Review panel
- Hematology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 2916657
- 3010131137
- 1618982
- 2244900
- 3010194621
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code GJG #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K831079 | LIQUIPETTE | The Kendall Company Div. of Tyco Healthcare Group | 1983-04-28 |
| K780237 | DISPOSABLE CONTROLLED DROP PASTEUR PIPET | Owens-Illinois, Inc. | 1978-03-09 |
| K760719 | UNIFORM DROP SIZE PASTEUR TYPE PIPETS | Dade, Baxter Travenol Diagnostics, Inc. | 1976-10-29 |
Legacy Summary#
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FDA Review#
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