The following data is part of a premarket notification filed by Camino Laboratories, Inc. with the FDA for Camino Model M420: Monit Inter W/mean Pres Display.
Device ID | K912833 |
510k Number | K912833 |
Device Name: | CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAY |
Classification | Computer, Blood-pressure |
Applicant | CAMINO LABORATORIES, INC. 5955 PACIFIC CENTER BLVD. San Diego, CA 92121 |
Contact | Marie Aker |
Correspondent | Marie Aker CAMINO LABORATORIES, INC. 5955 PACIFIC CENTER BLVD. San Diego, CA 92121 |
Product Code | DSK |
CFR Regulation Number | 870.1110 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-06-26 |
Decision Date | 1991-09-23 |