The following data is part of a premarket notification filed by Smith & Nephew United, Inc. with the FDA for Primapore I.v..
| Device ID | K893900 |
| 510k Number | K893900 |
| Device Name: | PRIMAPORE I.V. |
| Classification | Tape And Bandage, Adhesive |
| Applicant | SMITH & NEPHEW UNITED, INC. 11775 STARKLEY RD. P.O.BOX 1970 Largo, FL 34649 -1970 |
| Contact | Karen L Gerlach |
| Correspondent | Karen L Gerlach SMITH & NEPHEW UNITED, INC. 11775 STARKLEY RD. P.O.BOX 1970 Largo, FL 34649 -1970 |
| Product Code | KGX |
| CFR Regulation Number | 880.5240 [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-06-16 |
| Decision Date | 1989-08-03 |