The following data is part of a premarket notification filed by Sharp Electronics Corp. with the FDA for Model Mb-309h, Sharp Digital Blood Pressure Monito.
Device ID | K851664 |
510k Number | K851664 |
Device Name: | MODEL MB-309H, SHARP DIGITAL BLOOD PRESSURE MONITO |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | SHARP ELECTRONICS CORP. 10 SHARP PLAZA P.O. BOX 588 Paramus, NJ 07652 |
Contact | Glen Weinberg |
Correspondent | Glen Weinberg SHARP ELECTRONICS CORP. 10 SHARP PLAZA P.O. BOX 588 Paramus, NJ 07652 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-04-23 |
Decision Date | 1985-07-24 |