The following data is part of a premarket notification filed by Cabot Medical Corp. with the FDA for Cabot Fiber Laser Probe.
| Device ID | K873115 |
| 510k Number | K873115 |
| Device Name: | CABOT FIBER LASER PROBE |
| Classification | Laparoscope, Gynecologic (and Accessories) |
| Applicant | CABOT MEDICAL CORP. 2021 CABOT BOULEVARD WEST Langhorne, PA 19047 |
| Contact | Jack Keller |
| Correspondent | Jack Keller CABOT MEDICAL CORP. 2021 CABOT BOULEVARD WEST Langhorne, PA 19047 |
| Product Code | HET |
| CFR Regulation Number | 884.1720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-08-10 |
| Decision Date | 1988-01-28 |