The following data is part of a premarket notification filed by North American Instrument Corp. with the FDA for Morse Dt Manifold.
| Device ID | K902472 |
| 510k Number | K902472 |
| Device Name: | MORSE DT MANIFOLD |
| Classification | Transducer, Blood-pressure, Extravascular |
| Applicant | NORTH AMERICAN INSTRUMENT CORP. Glens Falls, NY 12801 |
| Contact | Robert E Franklin |
| Correspondent | Robert E Franklin NORTH AMERICAN INSTRUMENT CORP. Glens Falls, NY 12801 |
| Product Code | DRS |
| CFR Regulation Number | 870.2850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-06-04 |
| Decision Date | 1990-08-23 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10193489079005 | K902472 | 000 |
| 20193489065111 | K902472 | 000 |
| 20193489065104 | K902472 | 000 |
| 20193489065074 | K902472 | 000 |
| 20193489065050 | K902472 | 000 |
| 20193489065043 | K902472 | 000 |
| 20193489065012 | K902472 | 000 |
| 20193489064992 | K902472 | 000 |
| 20193489064985 | K902472 | 000 |
| 20193489065135 | K902472 | 000 |
| 20193489059004 | K902472 | 000 |
| 20193489059011 | K902472 | 000 |
| 10193489078992 | K902472 | 000 |
| 10193489067187 | K902472 | 000 |
| 10193489067170 | K902472 | 000 |
| 10193489066531 | K902472 | 000 |
| 10193489066524 | K902472 | 000 |
| 10193489066487 | K902472 | 000 |
| 10193489066470 | K902472 | 000 |
| 10193489059212 | K902472 | 000 |
| 20193489064947 | K902472 | 000 |