The following data is part of a premarket notification filed by Brant-wald Surgicals, Inc. with the FDA for Modified Sterilization Of Tur Aprons.
Device ID | K893634 |
510k Number | K893634 |
Device Name: | MODIFIED STERILIZATION OF TUR APRONS |
Classification | Mask, Surgical |
Applicant | BRANT-WALD SURGICALS, INC. P.O. BOX 4962 Oak Ridge, TN 37831 |
Contact | Rayburn C Waldrop |
Correspondent | Rayburn C Waldrop BRANT-WALD SURGICALS, INC. P.O. BOX 4962 Oak Ridge, TN 37831 |
Product Code | FXX |
CFR Regulation Number | 878.4040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-05-11 |
Decision Date | 1989-06-23 |