The following data is part of a premarket notification filed by Colon Therapeutics with the FDA for Modified Rectal Nozzle.
Device ID | K873948 |
510k Number | K873948 |
Device Name: | MODIFIED RECTAL NOZZLE |
Classification | Colonic Irrigation System |
Applicant | COLON THERAPEUTICS 2729 UPTON DR. Port Arthur, TX 77642 |
Contact | Jimmy Girouard |
Correspondent | Jimmy Girouard COLON THERAPEUTICS 2729 UPTON DR. Port Arthur, TX 77642 |
Product Code | KPL |
CFR Regulation Number | 876.5220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-09-28 |
Decision Date | 1987-10-14 |