510(k) K931145
K931145 is an FDA 510(k) premarket notification submitted by Amsco Sterile Recoveries, Inc. for the device "NON-STERILE ISOLATION GOWN". The FDA issued a decision of Substantially Equivalent on June 10, 1994. The device falls under product code FYC (Gown, Isolation, Surgical), a Class II device regulated under 21 CFR 878.4040. Amsco Sterile Recoveries, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 10, 1994
- Date Received
- March 5, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Gown, Isolation, Surgical
- Device Class
- Class II
- Regulation Number
- 878.4040
- Review Panel
- HO
- Submission Type