The following data is part of a premarket notification filed by Titan Mfg., Inc. with the FDA for Cushing Bayonet, Insulated Bipolar Forcep.
| Device ID | K974595 | 
| 510k Number | K974595 | 
| Device Name: | CUSHING BAYONET, INSULATED BIPOLAR FORCEP | 
| Classification | Forceps | 
| Applicant | TITAN MFG., INC. 6 JAMIE LN. Phoenixville, PA 19460 | 
| Contact | Donald Seavey | 
| Correspondent | Donald Seavey TITAN MFG., INC. 6 JAMIE LN. Phoenixville, PA 19460 | 
| Product Code | HTD | 
| CFR Regulation Number | 878.4800 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 1997-12-09 | 
| Decision Date | 1998-06-24 |