The following data is part of a premarket notification filed by Medical Research Laboratories, Inc. with the FDA for Dpd Defibrillator.
| Device ID | K930548 |
| 510k Number | K930548 |
| Device Name: | DPD DEFIBRILLATOR |
| Classification | Dc-defibrillator, Low-energy, (including Paddles) |
| Applicant | MEDICAL RESEARCH LABORATORIES, INC. 1000 ASBURY DR. NO.17 Buffalo Grove, IL 60089 |
| Contact | Dilip Mehta |
| Correspondent | Dilip Mehta MEDICAL RESEARCH LABORATORIES, INC. 1000 ASBURY DR. NO.17 Buffalo Grove, IL 60089 |
| Product Code | LDD |
| CFR Regulation Number | 870.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-02-03 |
| Decision Date | 1993-06-25 |