The following data is part of a premarket notification filed by Camino Laboratories, Inc. with the FDA for Ventricular Bolt Pressure Monitoring Kit #110-4h.
Device ID | K881183 |
510k Number | K881183 |
Device Name: | VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H |
Classification | Device, Monitoring, Intracranial Pressure |
Applicant | CAMINO LABORATORIES, INC. 5955 PACIFIC CENTER BLVD. San Diego, CA 92121 |
Contact | Dan Mckay |
Correspondent | Dan Mckay CAMINO LABORATORIES, INC. 5955 PACIFIC CENTER BLVD. San Diego, CA 92121 |
Product Code | GWM |
CFR Regulation Number | 882.1620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-03-21 |
Decision Date | 1988-05-04 |