510(k) K770372
K770372 is an FDA 510(k) premarket notification submitted by Castle Co. for the device "STERILIZER, STEAM, CASTLE 3000". The FDA issued a decision of Substantially Equivalent on April 5, 1977. The device falls under product code FLE (Sterilizer, Steam), a Class II device regulated under 21 CFR 880.6880. Castle Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 5, 1977
- Date Received
- February 25, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sterilizer, Steam
- Device Class
- Class II
- Regulation Number
- 880.6880
- Review Panel
- HO
- Submission Type