510(k) K944333
K944333 is an FDA 510(k) premarket notification submitted by Wilshire Medical Products for the device "HYDRODERM GEL WOUND DRESSING". The FDA issued a decision of SN on November 10, 1994. The device falls under product code MGQ (Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic), a Class U device. Wilshire Medical Products has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- November 10, 1994
- Date Received
- September 6, 1994
- 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