510(k) K791893
- Device
- 19091-XXXXX SER. OF GLASS CAPILLARY COL.
- Applicant
- HEWLETT-PACKARD CO.
- 510(k) number
- K791893
- Product code
- DII
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1979-10-30
- Date received
- 1979-09-25
- Regulation
- 862.2250
- Classification name
- Columns, Glc
- Medical specialty
- Clinical Chemistry
- Review panel
- Toxicology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code DII #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K874824 | CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY | Supelco, Inc. | 1988-01-21 |
| K862542 | CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY | Supelco, Inc. | 1986-08-04 |
| K844164 | REACTIFS, IBF ULTROGELS ACA & ULTROGELS A | Lkb Instruments, Inc. | 1984-12-10 |
| K841712 | CAPILLARY GAS CHROMATOGRAPHIC COLUMNS | Supelco, Inc. | 1984-05-21 |
Legacy Summary#
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FDA Review#
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