The following data is part of a premarket notification filed by Consolidated Medical Equipment, Inc. with the FDA for Closed Wound Drain.
Device ID | K850037 |
510k Number | K850037 |
Device Name: | CLOSED WOUND DRAIN |
Classification | Apparatus, Suction, Single Patient Use, Portable, Nonpowered |
Applicant | CONSOLIDATED MEDICAL EQUIPMENT, INC. 310 BROAD ST. Utica, NY 13501 |
Contact | William W Abraham |
Correspondent | William W Abraham CONSOLIDATED MEDICAL EQUIPMENT, INC. 310 BROAD ST. Utica, NY 13501 |
Product Code | GCY |
CFR Regulation Number | 878.4680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-01-07 |
Decision Date | 1985-03-19 |