The following data is part of a premarket notification filed by James River Corp. with the FDA for Caretex Central Supply Wrap.
Device ID | K883802 |
510k Number | K883802 |
Device Name: | CARETEX CENTRAL SUPPLY WRAP |
Classification | Wrap, Sterilization |
Applicant | JAMES RIVER CORP. 1915 MARATHON AVE. Neenah, WI 54956 |
Contact | Richard L Davis |
Correspondent | Richard L Davis JAMES RIVER CORP. 1915 MARATHON AVE. Neenah, WI 54956 |
Product Code | FRG |
CFR Regulation Number | 880.6850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-09-07 |
Decision Date | 1988-10-21 |