510(k) K032631
K032631 is an FDA 510(k) premarket notification submitted by Lac Mac, Ltd. for the device "INNERBLOC LR SURGICAL GOWNS BASED ON GORE LR FABRIC (REUSABLE 100X)". The FDA issued a decision of Substantially Equivalent on Feb 5, 2004. The device falls under product code FYA (Gown, Surgical), a Class II device regulated under 21 CFR 878.4040. Lac Mac, Ltd. has 5 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 5, 2004
- Date Received
- Aug 26, 2003
- 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)