510(k) K172850
K172850 is an FDA 510(k) premarket notification submitted by Aesculap, Inc. for the device "SterilContainer with PrimeLine Pro Lid". The FDA issued a decision of Substantially Equivalent on Nov 17, 2017. The device falls under product code KCT (Sterilization Wrap Containers, Trays, Cassettes & Other Accessories), a Class II device regulated under 21 CFR 880.6850. Aesculap, Inc. has 217 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 17, 2017
- Date Received
- Sep 20, 2017
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
- Device Class
- Class II
- Regulation Number
- 880.6850
- Review Panel
- HO
- Submission Type
- 510(k)