The following data is part of a premarket notification filed by Diag Corp. with the FDA for Disposable Patient Cable.
| Device ID | K910645 |
| 510k Number | K910645 |
| Device Name: | DISPOSABLE PATIENT CABLE |
| Classification | Cable, Transducer And Electrode, Patient, (including Connector) |
| Applicant | DIAG CORP. 14901 DEVEAU PLACE Minnetonka, MN 55345 -2126 |
| Contact | J Fleischhacker |
| Correspondent | J Fleischhacker DIAG CORP. 14901 DEVEAU PLACE Minnetonka, MN 55345 -2126 |
| Product Code | DSA |
| CFR Regulation Number | 870.2900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-02-13 |
| Decision Date | 1991-05-07 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 15414734054253 | K910645 | 000 |
| 15414734053676 | K910645 | 000 |
| 15414734053652 | K910645 | 000 |
| 15414734022146 | K910645 | 000 |
| 15414734020043 | K910645 | 000 |
| 15414734009673 | K910645 | 000 |