The following data is part of a premarket notification filed by Rudolf Riester Gmbh & Co. Kg with the FDA for Minimus Ii; Minimus Ii Color; Babyphon.
| Device ID | K942777 |
| 510k Number | K942777 |
| Device Name: | MINIMUS II; MINIMUS II COLOR; BABYPHON |
| Classification | Blood Pressure Cuff |
| Applicant | RUDOLF RIESTER GMBH & CO. KG POSTFACH 35 BRUCKSTRABE 31 D-72417 Jungingen, DE |
| Contact | Karlheinz Riester |
| Correspondent | Karlheinz Riester RUDOLF RIESTER GMBH & CO. KG POSTFACH 35 BRUCKSTRABE 31 D-72417 Jungingen, DE |
| Product Code | DXQ |
| CFR Regulation Number | 870.1120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-05-31 |
| Decision Date | 1994-07-27 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04045396215566 | K942777 | 000 |
| 04045396102644 | K942777 | 000 |
| 04045396106802 | K942777 | 000 |
| 04045396109452 | K942777 | 000 |
| 04045396109513 | K942777 | 000 |
| 04045396126145 | K942777 | 000 |
| 04045396155305 | K942777 | 000 |
| 04045396209992 | K942777 | 000 |
| 04045396215511 | K942777 | 000 |
| 04045396215528 | K942777 | 000 |
| 04045396215542 | K942777 | 000 |
| 04045396102439 | K942777 | 000 |