510(k) K220333
K220333 is an FDA 510(k) premarket notification submitted by Medline Industries, LP for the device "Medline Orbis LVL 3 Surgical Gown". The FDA issued a decision of Substantially Equivalent on May 18, 2022. The device falls under product code FYA (Gown, Surgical), a Class II device regulated under 21 CFR 878.4040. Medline Industries, LP has 268 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 18, 2022
- Date Received
- Feb 4, 2022
- 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)