The following data is part of a premarket notification filed by Cadwell Laboratories, Inc. with the FDA for Disposable Tab Electrode.
| Device ID | K933803 |
| 510k Number | K933803 |
| Device Name: | DISPOSABLE TAB ELECTRODE |
| Classification | Electrode, Cutaneous |
| Applicant | CADWELL LABORATORIES, INC. 909 NORTH KELLOGG ST. Kennewick, WA 99336 |
| Contact | Carlton M Cadwell |
| Correspondent | Carlton M Cadwell CADWELL LABORATORIES, INC. 909 NORTH KELLOGG ST. Kennewick, WA 99336 |
| Product Code | GXY |
| CFR Regulation Number | 882.1320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-08-04 |
| Decision Date | 1994-07-08 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20840067101418 | K933803 | 000 |
| 10840067100902 | K933803 | 000 |
| 10840067100896 | K933803 | 000 |
| 10840067100889 | K933803 | 000 |
| 10840067100872 | K933803 | 000 |
| 10840067100865 | K933803 | 000 |
| 10840067100858 | K933803 | 000 |
| 10840067100841 | K933803 | 000 |
| 10840067100834 | K933803 | 000 |
| 10840067100827 | K933803 | 000 |
| 10840067100810 | K933803 | 000 |
| 10840067100919 | K933803 | 000 |
| 10840067100926 | K933803 | 000 |
| 10840067101411 | K933803 | 000 |
| 20840067101401 | K933803 | 000 |
| 10840067101398 | K933803 | 000 |
| 10840067101381 | K933803 | 000 |
| 10840067101374 | K933803 | 000 |
| 00840067101360 | K933803 | 000 |
| 10840067101343 | K933803 | 000 |
| 10840067101244 | K933803 | 000 |
| 10840067101169 | K933803 | 000 |
| 00840067103913 | K933803 | 000 |
| 00840067103890 | K933803 | 000 |
| 10840067100803 | K933803 | 000 |