The following data is part of a premarket notification filed by Apollo Products, Inc. with the FDA for Apollo Heart Rate Indicator.
| Device ID | K790999 |
| 510k Number | K790999 |
| Device Name: | APOLLO HEART RATE INDICATOR |
| Classification | Plethysmograph, Photoelectric, Pneumatic Or Hydraulic |
| Applicant | APOLLO PRODUCTS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | JOM |
| CFR Regulation Number | 870.2780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-05-29 |
| Decision Date | 1979-06-22 |