The following data is part of a premarket notification filed by Propper Mfg. Co., Inc. with the FDA for Propper Laryngoscope Blades W Fiber Optic Illum..
| Device ID | K915804 |
| 510k Number | K915804 |
| Device Name: | PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM. |
| Classification | Laryngoscope, Rigid |
| Applicant | PROPPER MFG. CO., INC. 3604 SKILLMAN AVE. Long Island City, NY 11101 |
| Contact | Kenneth Summer |
| Correspondent | Kenneth Summer PROPPER MFG. CO., INC. 3604 SKILLMAN AVE. Long Island City, NY 11101 |
| Product Code | CCW |
| CFR Regulation Number | 868.5540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-12-24 |
| Decision Date | 1992-03-20 |