The following data is part of a premarket notification filed by Thantex Specialties, Inc. with the FDA for Orex(r) O.r Equipment Drapes.
Device ID | K945755 |
510k Number | K945755 |
Device Name: | OREX(R) O.R EQUIPMENT DRAPES |
Classification | Drape, Surgical |
Applicant | THANTEX SPECIALTIES, INC. 251 EXCHANGE PLACE Herndon, VA 22070 -4822 |
Contact | Tom Bonner |
Correspondent | Tom Bonner THANTEX SPECIALTIES, INC. 251 EXCHANGE PLACE Herndon, VA 22070 -4822 |
Product Code | KKX |
CFR Regulation Number | 878.4370 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-11-23 |
Decision Date | 1995-05-25 |