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 |