510(k) K800528
K800528 is an FDA 510(k) premarket notification submitted by American Convertors Div., American Pharmaseal for the device "SHIELD PERFECT FIT; DURA-FIT, DISPOS.". The FDA issued a decision of Substantially Equivalent on April 16, 1980. The device falls under product code FXP (Cover, Shoe, Operating-Room), a Class I device regulated under 21 CFR 878.4040. American Convertors Div., American Pharmaseal has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 16, 1980
- Date Received
- March 7, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cover, Shoe, Operating-Room
- Device Class
- Class I
- Regulation Number
- 878.4040
- Review Panel
- HO
- Submission Type