510(k) K993119

STERILE HYDROGEL by Dumex Medical Surgical Products, Ltd. — Product Code MGQ

K993119 is an FDA 510(k) premarket notification submitted by Dumex Medical Surgical Products, Ltd. for the device "STERILE HYDROGEL". The FDA issued a decision of Substantially Equivalent on November 23, 1999. The device falls under product code MGQ (Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic), a Class U device. Dumex Medical Surgical Products, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 23, 1999
Date Received
September 20, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type