The following data is part of a premarket notification filed by North American Instrument Corp. with the FDA for Morse Anesthesia.
| Device ID | K905208 |
| 510k Number | K905208 |
| Device Name: | MORSE ANESTHESIA |
| Classification | Set, Administration, Intravascular |
| Applicant | NORTH AMERICAN INSTRUMENT CORP. Glens Falls, NY 12801 |
| Contact | Robert Franklin |
| Correspondent | Robert Franklin NORTH AMERICAN INSTRUMENT CORP. Glens Falls, NY 12801 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-11-20 |
| Decision Date | 1992-01-10 |