The following data is part of a premarket notification filed by Cabot Medical Corp. with the FDA for Cabot Medical Bipolar Cutting Forceps.
| Device ID | K932293 |
| 510k Number | K932293 |
| Device Name: | CABOT MEDICAL BIPOLAR CUTTING FORCEPS |
| Classification | Unit, Electrosurgical, Endoscopic (with Or Without Accessories) |
| Applicant | CABOT MEDICAL CORP. 2021 CABOT BOULEVARD WEST Langhorne, PA 19047 |
| Contact | Todd Polk |
| Correspondent | Todd Polk CABOT MEDICAL CORP. 2021 CABOT BOULEVARD WEST Langhorne, PA 19047 |
| Product Code | KNS |
| CFR Regulation Number | 876.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-05-11 |
| Decision Date | 1994-07-27 |