The following data is part of a premarket notification filed by Tico Medical Instruments, Inc. with the FDA for Vital Signs Monitor.
Device ID | K884938 |
510k Number | K884938 |
Device Name: | VITAL SIGNS MONITOR |
Classification | Computer, Blood-pressure |
Applicant | TICO MEDICAL INSTRUMENTS, INC. 3600 STATE RD 520 P.O. BOX 3823 Cocoa, FL 32926 |
Contact | E. J Simicich |
Correspondent | E. J Simicich TICO MEDICAL INSTRUMENTS, INC. 3600 STATE RD 520 P.O. BOX 3823 Cocoa, FL 32926 |
Product Code | DSK |
CFR Regulation Number | 870.1110 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-11-28 |
Decision Date | 1989-04-19 |