The following data is part of a premarket notification filed by Pentax Precision Instrument Corp. with the FDA for Fi-10p.
| Device ID | K951195 |
| 510k Number | K951195 |
| Device Name: | FI-10P |
| Classification | Laryngoscope, Non-rigid |
| Applicant | PENTAX PRECISION INSTRUMENT CORP. 3117 COMMERCE PKWY. Miramar, FL 33025 |
| Contact | Paul Silva |
| Correspondent | Paul Silva PENTAX PRECISION INSTRUMENT CORP. 3117 COMMERCE PKWY. Miramar, FL 33025 |
| Product Code | CAL |
| CFR Regulation Number | 868.5530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-03-16 |
| Decision Date | 1995-04-06 |