The following data is part of a premarket notification filed by Liaoning-usa Corp. with the FDA for Various Types Of Stethoscopes.
| Device ID | K905487 |
| 510k Number | K905487 |
| Device Name: | VARIOUS TYPES OF STETHOSCOPES |
| Classification | Stethoscope, Manual |
| Applicant | LIAONING-USA CORP. 123 WEST BELLEVUE, UNIT#4 Pasadena, CA 91105 -2549 |
| Contact | Jay A Brown |
| Correspondent | Jay A Brown LIAONING-USA CORP. 123 WEST BELLEVUE, UNIT#4 Pasadena, CA 91105 -2549 |
| Product Code | LDE |
| CFR Regulation Number | 870.1875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-12-06 |
| Decision Date | 1991-04-09 |