The following data is part of a premarket notification filed by Johnson & Johnson Professionals, Inc. with the FDA for Johnson & Johnson Absorbent Occlusive Dressing.
Device ID | K872982 |
510k Number | K872982 |
Device Name: | JOHNSON & JOHNSON ABSORBENT OCCLUSIVE DRESSING |
Classification | Dressing, Wound, Drug |
Applicant | JOHNSON & JOHNSON PROFESSIONALS, INC. 325 PARAMOUNT DR. Raynham, MA 02767 -0350 |
Contact | Omega Norton-crable |
Correspondent | Omega Norton-crable JOHNSON & JOHNSON PROFESSIONALS, INC. 325 PARAMOUNT DR. Raynham, MA 02767 -0350 |
Product Code | FRO |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-07-31 |
Decision Date | 1987-08-14 |