510(k) K920516
K920516 is an FDA 510(k) premarket notification submitted by Trinity Laboratories, Inc. for the device "GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB". The FDA issued a decision of Substantially Equivalent (kit, denovo) on April 16, 1992. The device falls under product code KDD (Kit, Surgical Instrument, Disposable), a Class I device regulated under 21 CFR 878.4800. Trinity Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SEKD (Substantially Equivalent (kit, denovo))
- Decision Date
- April 16, 1992
- Date Received
- February 4, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Surgical Instrument, Disposable
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type