The following data is part of a premarket notification filed by Industrial & Biomedical Sensors Corp. with the FDA for Cm-700a Auto-inflate Control Module.
Device ID | K802203 |
510k Number | K802203 |
Device Name: | CM-700A AUTO-INFLATE CONTROL MODULE |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | INDUSTRIAL & BIOMEDICAL SENSORS CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1980-09-11 |
Decision Date | 1980-10-03 |