510(k) K042285
K042285 is an FDA 510(k) premarket notification submitted by United Medical Industries Co. , Ltd. for the device "UNICRYL M". The FDA issued a decision of Substantially Equivalent on December 10, 2004. The device falls under product code NEW (Suture, Surgical, Absorbable, Polydioxanone), a Class II device regulated under 21 CFR 878.4840. United Medical Industries Co. , Ltd. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 10, 2004
- Date Received
- August 24, 2004
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Suture, Surgical, Absorbable, Polydioxanone
- Device Class
- Class II
- Regulation Number
- 878.4840
- Review Panel
- SU
- Submission Type