The following data is part of a premarket notification filed by Coast Medical, Inc. with the FDA for Surface Temperature Probes.
Device ID | K943270 |
510k Number | K943270 |
Device Name: | SURFACE TEMPERATURE PROBES |
Classification | Thermometer, Electronic, Clinical |
Applicant | COAST MEDICAL, INC. 1060 NORTH BATAVIA UNIT H Orange, CA 92667 |
Contact | Douglas R Mongeon |
Correspondent | Douglas R Mongeon COAST MEDICAL, INC. 1060 NORTH BATAVIA UNIT H Orange, CA 92667 |
Product Code | FLL |
CFR Regulation Number | 880.2910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-07-07 |
Decision Date | 1994-12-05 |