The following data is part of a premarket notification filed by Ct Intl. with the FDA for Nitrilon Correct-touch.
Device ID | K984512 |
510k Number | K984512 |
Device Name: | NITRILON CORRECT-TOUCH |
Classification | Surgeon's Gloves |
Applicant | CT INTL. 4349 SANTA FE RD. San Luis Obispo, CA 93401 |
Contact | Mike Kyle |
Correspondent | Mike Kyle CT INTL. 4349 SANTA FE RD. San Luis Obispo, CA 93401 |
Product Code | KGO |
CFR Regulation Number | 878.4460 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-12-18 |
Decision Date | 1999-07-12 |