The following data is part of a premarket notification filed by Deroyal Industries, Inc. with the FDA for Qualtex Skin Staple Extractor.
Device ID | K911204 |
510k Number | K911204 |
Device Name: | QUALTEX SKIN STAPLE EXTRACTOR |
Classification | Staple, Removable (skin) |
Applicant | DEROYAL INDUSTRIES, INC. 200 DEBUSK LN. Powell, TN 37849 |
Contact | Debusk Lane |
Correspondent | Debusk Lane DEROYAL INDUSTRIES, INC. 200 DEBUSK LN. Powell, TN 37849 |
Product Code | GDT |
CFR Regulation Number | 878.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-03-19 |
Decision Date | 1991-05-08 |