510(k) K010825
K010825 is an FDA 510(k) premarket notification submitted by Medline for the device "MEDLINE STERISET STERILIZATION CONTAINER". The FDA issued a decision of Substantially Equivalent on May 8, 2001. The device falls under product code FRG (Wrap, Sterilization), a Class II device regulated under 21 CFR 880.6850. Medline has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 8, 2001
- Date Received
- March 19, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wrap, Sterilization
- Device Class
- Class II
- Regulation Number
- 880.6850
- Review Panel
- HO
- Submission Type