The following data is part of a premarket notification filed by Rud Riester Gmbh & Co Kg with the FDA for Various Stethoscopes.
| Device ID | K944337 |
| 510k Number | K944337 |
| Device Name: | VARIOUS STETHOSCOPES |
| Classification | Stethoscope, Manual |
| Applicant | RUD RIESTER GMBH & CO KG BRUCKSTR.31,P.O.BOX 35 Jungingen, DE |
| Contact | Karlheinz Riester |
| Correspondent | Karlheinz Riester RUD RIESTER GMBH & CO KG BRUCKSTR.31,P.O.BOX 35 Jungingen, DE |
| Product Code | LDE |
| CFR Regulation Number | 870.1875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-09-06 |
| Decision Date | 1994-11-30 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04045396212749 | K944337 | 000 |
| 04045396177390 | K944337 | 000 |
| 04045396163546 | K944337 | 000 |
| 04045396119857 | K944337 | 000 |
| 04045396119833 | K944337 | 000 |
| 04045396119826 | K944337 | 000 |
| 04045396118867 | K944337 | 000 |
| 04045396118683 | K944337 | 000 |
| 04045396118492 | K944337 | 000 |
| 04045396118485 | K944337 | 000 |
| 04045396006454 | K944337 | 000 |
| 04045396006430 | K944337 | 000 |
| 04045396006355 | K944337 | 000 |
| 04045396006348 | K944337 | 000 |
| 04045396006324 | K944337 | 000 |
| 04045396006317 | K944337 | 000 |
| 04045396177406 | K944337 | 000 |
| 04045396195370 | K944337 | 000 |
| 04045396195387 | K944337 | 000 |
| 04045396195561 | K944337 | 000 |
| 04045396195547 | K944337 | 000 |
| 04045396195530 | K944337 | 000 |
| 04045396195523 | K944337 | 000 |
| 04045396195509 | K944337 | 000 |
| 04045396195493 | K944337 | 000 |
| 04045396195486 | K944337 | 000 |
| 04045396195479 | K944337 | 000 |
| 04045396195462 | K944337 | 000 |
| 04045396195448 | K944337 | 000 |
| 04045396195431 | K944337 | 000 |
| 04045396195424 | K944337 | 000 |
| 04045396195417 | K944337 | 000 |
| 04045396195400 | K944337 | 000 |
| 04045396195394 | K944337 | 000 |
| 04045396000186 | K944337 | 000 |