The following data is part of a premarket notification filed by Deroyal Industries, Inc. with the FDA for Qualtex Magnetic Instrument Drape.
Device ID | K914369 |
510k Number | K914369 |
Device Name: | QUALTEX MAGNETIC INSTRUMENT DRAPE |
Classification | Drape, Surgical |
Applicant | DEROYAL INDUSTRIES, INC. 200 DEBUSK LN. Powell, TN 37849 |
Contact | Debra F.manning |
Correspondent | Debra F.manning DEROYAL INDUSTRIES, INC. 200 DEBUSK LN. Powell, TN 37849 |
Product Code | KKX |
CFR Regulation Number | 878.4370 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-10-01 |
Decision Date | 1991-12-02 |