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 |