The following data is part of a premarket notification filed by Johnson & Johnson Professionals, Inc. with the FDA for Ultrasound Imaging System Model 280 Sl.
Device ID | K860697 |
510k Number | K860697 |
Device Name: | ULTRASOUND IMAGING SYSTEM MODEL 280 SL |
Classification | System, Imaging, Pulsed Echo, Ultrasonic |
Applicant | JOHNSON & JOHNSON PROFESSIONALS, INC. 69 SPRING ST. Ramsey, NJ 07446 |
Contact | Raymond F Chase |
Correspondent | Raymond F Chase JOHNSON & JOHNSON PROFESSIONALS, INC. 69 SPRING ST. Ramsey, NJ 07446 |
Product Code | IYO |
CFR Regulation Number | 892.1560 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-02-25 |
Decision Date | 1986-07-24 |