510(k) K944138
K944138 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "INTERWOVEN OPTIGUARD REUSABLE GOWN MATERIAL". The FDA issued a decision of Substantially Equivalent on Dec 20, 1994. The device falls under product code FYA (Gown, Surgical), a Class II device regulated under 21 CFR 878.4040. Baxter Healthcare Corp has 507 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 20, 1994
- Date Received
- Aug 24, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Gown, Surgical
- Device Class
- Class II
- Regulation Number
- 878.4040
- Review Panel
- HO
- Submission Type
- 510(k)