The following data is part of a premarket notification filed by Ohio Medical Products with the FDA for Flowmeter, P.c., Redesigned Version.
| Device ID | K760102 |
| 510k Number | K760102 |
| Device Name: | FLOWMETER, P.C., REDESIGNED VERSION |
| Classification | Flowmeter, Tube, Thorpe, Back-pressure Compensated |
| Applicant | OHIO MEDICAL PRODUCTS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CAX |
| CFR Regulation Number | 868.2340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-06-23 |
| Decision Date | 1976-07-16 |