The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Dispos. Pressure Kit 1295k Series.
Device ID | K843273 |
510k Number | K843273 |
Device Name: | DISPOS. PRESSURE KIT 1295K SERIES |
Classification | Transducer, Blood-pressure, Extravascular |
Applicant | HEWLETT-PACKARD CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | DRS |
CFR Regulation Number | 870.2850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-08-20 |
Decision Date | 1985-06-11 |