The following data is part of a premarket notification filed by Micro Medical, Ltd. with the FDA for Veripoid 50 Bio-electrical Impedance Meter.
| Device ID | K881851 |
| 510k Number | K881851 |
| Device Name: | VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER |
| Classification | Plethysmograph, Impedance |
| Applicant | MICRO MEDICAL, LTD. SUITE 972 200 S.W. MARKET Portland, OR 97201 |
| Contact | William Weinstein |
| Correspondent | William Weinstein MICRO MEDICAL, LTD. SUITE 972 200 S.W. MARKET Portland, OR 97201 |
| Product Code | DSB |
| CFR Regulation Number | 870.2770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-05-02 |
| Decision Date | 1988-09-26 |