510(k) K881447
K881447 is an FDA 510(k) premarket notification submitted by Metatech Corp. for the device "METATECH METAL MICROCLIP". The FDA issued a decision of Substantially Equivalent on June 22, 1988. The device falls under product code DXC (Clamp, Vascular), a Class II device regulated under 21 CFR 870.4450. Metatech Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 22, 1988
- Date Received
- April 6, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Clamp, Vascular
- Device Class
- Class II
- Regulation Number
- 870.4450
- Review Panel
- CV
- Submission Type