The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for 19091-xxxxx Ser. Of Glass Capillary Col..
| Device ID | K791893 |
| 510k Number | K791893 |
| Device Name: | 19091-XXXXX SER. OF GLASS CAPILLARY COL. |
| Classification | Columns, Glc |
| Applicant | HEWLETT-PACKARD CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DII |
| CFR Regulation Number | 862.2250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-09-25 |
| Decision Date | 1979-10-30 |