The following data is part of a premarket notification filed by North American Instrument Corp. with the FDA for The Perceptor(tm) Stand Alone Transducer.
| Device ID | K910764 |
| 510k Number | K910764 |
| Device Name: | THE PERCEPTOR(TM) STAND ALONE TRANSDUCER |
| 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 | 1991-01-31 |
| Decision Date | 1991-04-22 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| H965800300130 | K910764 | 000 |
| 20193489066118 | K910764 | 000 |
| 20193489066125 | K910764 | 000 |
| 20193489066132 | K910764 | 000 |
| 20193489064640 | K910764 | 000 |
| 20193489064657 | K910764 | 000 |
| 20193489064664 | K910764 | 000 |
| 20193489064671 | K910764 | 000 |
| 10193489064780 | K910764 | 000 |
| 10193489064797 | K910764 | 000 |
| 10193489066272 | K910764 | 000 |
| H965800300521 | K910764 | 000 |
| 30193489064807 | K910764 | 000 |