The following data is part of a premarket notification filed by Applied Medical Research with the FDA for Dinamap Model 846.
Device ID | K781053 |
510k Number | K781053 |
Device Name: | DINAMAP MODEL 846 |
Classification | Computer, Blood-pressure |
Applicant | APPLIED MEDICAL RESEARCH 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | DSK |
CFR Regulation Number | 870.1110 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-06-22 |
Decision Date | 1978-09-07 |