The following data is part of a premarket notification filed by Molnlycke Health Care, Inc. with the FDA for Klinidrape Surgical Drapes.
Device ID | K000906 |
510k Number | K000906 |
Device Name: | KLINIDRAPE SURGICAL DRAPES |
Classification | Drape, Surgical |
Applicant | MOLNLYCKE HEALTH CARE, INC. 500 BALDWIN TOWER Eddystone, PA 19022 |
Contact | Miguel A Negron |
Correspondent | Miguel A Negron MOLNLYCKE HEALTH CARE, INC. 500 BALDWIN TOWER Eddystone, PA 19022 |
Product Code | KKX |
CFR Regulation Number | 878.4370 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-03-21 |
Decision Date | 2000-06-23 |