510(k) K202447
K202447 is an FDA 510(k) premarket notification submitted by Medline Industries, Inc. for the device "Medline Orbis Surgical Gown". The FDA issued a decision of Substantially Equivalent on Apr 2, 2021. The device falls under product code FYA (Gown, Surgical), a Class II device regulated under 21 CFR 878.4040. Medline Industries, Inc. has 268 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 2, 2021
- Date Received
- Aug 26, 2020
- 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)