The following data is part of a premarket notification filed by Draeger Medical Ag & Co. Kg with the FDA for Nbp Cuff.
| Device ID | K092999 |
| 510k Number | K092999 |
| Device Name: | NBP CUFF |
| Classification | Blood Pressure Cuff |
| Applicant | DRAEGER MEDICAL AG & CO. KG 3135 Quarry Road Telford, PA 18969 |
| Contact | Joyce Kilroy |
| Correspondent | Joyce Kilroy DRAEGER MEDICAL AG & CO. KG 3135 Quarry Road Telford, PA 18969 |
| Product Code | DXQ |
| CFR Regulation Number | 870.1120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-09-28 |
| Decision Date | 2009-11-24 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04048675042198 | K092999 | 000 |
| 04048675042020 | K092999 | 000 |
| 04048675042013 | K092999 | 000 |
| 04048675042006 | K092999 | 000 |
| 04048675041993 | K092999 | 000 |
| 04048675041986 | K092999 | 000 |
| 04048675252009 | K092999 | 000 |
| 04048675428947 | K092999 | 000 |
| 04048675267706 | K092999 | 000 |
| 04048675042037 | K092999 | 000 |
| 04048675042044 | K092999 | 000 |
| 04048675042051 | K092999 | 000 |
| 04048675042167 | K092999 | 000 |
| 04048675042150 | K092999 | 000 |
| 04048675042143 | K092999 | 000 |
| 04048675042136 | K092999 | 000 |
| 04048675042129 | K092999 | 000 |
| 04048675042112 | K092999 | 000 |
| 04048675042105 | K092999 | 000 |
| 04048675042075 | K092999 | 000 |
| 04048675042273 | K092999 | 000 |