The following data is part of a premarket notification filed by Parke-davis Co. with the FDA for Aeroplast Dressing.
| Device ID | K781031 |
| 510k Number | K781031 |
| Device Name: | AEROPLAST DRESSING |
| Classification | Bandage, Liquid |
| Applicant | PARKE-DAVIS CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KMF |
| CFR Regulation Number | 880.5090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-06-19 |
| Decision Date | 1978-07-27 |