The following data is part of a premarket notification filed by Syncor Intl. Corp. with the FDA for Wire Cutters, Brachytherapy-table Top & Hand Held.
| Device ID | K850726 |
| 510k Number | K850726 |
| Device Name: | WIRE CUTTERS, BRACHYTHERAPY-TABLE TOP & HAND HELD |
| Classification | Source, Wire, Iridium, Radioactive |
| Applicant | SYNCOR INTL. CORP. 12847 ARROYO ST. Sylmar, CA 91342 |
| Contact | Eleanor V Chiu |
| Correspondent | Eleanor V Chiu SYNCOR INTL. CORP. 12847 ARROYO ST. Sylmar, CA 91342 |
| Product Code | IWA |
| CFR Regulation Number | 892.5730 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-02-22 |
| Decision Date | 1985-03-26 |