Johnson & Johnson Medical, Inc. · Class I · Cleared Dec 31, 1996
| K-number | K964016 |
| Device name | TIELLE HYDROPOLYMER FOAM DRESSING |
| Applicant | Johnson & Johnson Medical, Inc. |
| Product code | KMF |
| Device class | Class I |
| Decision date | Dec 31, 1996 |
| Decision | Substantially Equivalent for Some Indications |
| Regulation | 880.5090 |
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