510(k) K931618
K931618 is an FDA 510(k) premarket notification submitted by Convatec, A Division of E.R. Squibb & Sons for the device "DUODERM HYDROCOLLOID GEL". The FDA issued a decision of Substantially Equivalent on December 10, 1993. The device falls under product code NAE (Dressing, Wound, Hydrogel Without Drug And/Or Biologic), a Class I device regulated under 21 CFR 878.4022. Convatec, A Division of E.R. Squibb & Sons has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 10, 1993
- Date Received
- April 2, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dressing, Wound, Hydrogel Without Drug And/Or Biologic
- Device Class
- Class I
- Regulation Number
- 878.4022
- Review Panel
- SU
- Submission Type