The following data is part of a premarket notification filed by Nihon Kohden America, Inc. with the FDA for Cardiolife Tec-7300 W/optional Accessories.
| Device ID | K880575 |
| 510k Number | K880575 |
| Device Name: | CARDIOLIFE TEC-7300 W/OPTIONAL ACCESSORIES |
| Classification | Dc-defibrillator, Low-energy, (including Paddles) |
| Applicant | NIHON KOHDEN AMERICA, INC. 17112 ARMSTRONG AVE. Irvine, CA 92714 |
| Contact | Mike Dashefsky |
| Correspondent | Mike Dashefsky NIHON KOHDEN AMERICA, INC. 17112 ARMSTRONG AVE. Irvine, CA 92714 |
| Product Code | LDD |
| CFR Regulation Number | 870.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-02-10 |
| Decision Date | 1988-08-02 |