The following data is part of a premarket notification filed by Travenol Laboratories, S.a. with the FDA for Solution Administration Sets.
| Device ID | K860272 |
| 510k Number | K860272 |
| Device Name: | SOLUTION ADMINISTRATION SETS |
| Classification | Set, Administration, Intravascular |
| Applicant | TRAVENOL LABORATORIES, S.A. Deerfield, IL 60015 |
| Contact | Brian Stembal |
| Correspondent | Brian Stembal TRAVENOL LABORATORIES, S.A. Deerfield, IL 60015 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-01-27 |
| Decision Date | 1986-03-18 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50085412014666 | K860272 | 000 |