The following data is part of a premarket notification filed by Richard Hamer Assoc., Inc. with the FDA for Costello-everett Laser Cystoscope Sheath.
| Device ID | K942573 |
| 510k Number | K942573 |
| Device Name: | COSTELLO-EVERETT LASER CYSTOSCOPE SHEATH |
| Classification | Endoscopic Access Overtube, Gastroenterology-urology |
| Applicant | RICHARD HAMER ASSOC., INC. P.O. BOX 16598 Ft. Worth, TX 76162 -0598 |
| Contact | Richard A Hamer |
| Correspondent | Richard A Hamer RICHARD HAMER ASSOC., INC. P.O. BOX 16598 Ft. Worth, TX 76162 -0598 |
| Product Code | FED |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-05-31 |
| Decision Date | 1994-07-18 |