510(k) K972190
K972190 is an FDA 510(k) premarket notification submitted by American Laboratory Products Co., Ltd. for the device "THYROGLOBULIN ASSAY SYSTEM". The FDA issued a decision of Substantially Equivalent on July 14, 1997. The device falls under product code JZO (System, Test, Thyroid Autoantibody), a Class II device regulated under 21 CFR 866.5870. American Laboratory Products Co., Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 14, 1997
- Date Received
- May 19, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Test, Thyroid Autoantibody
- Device Class
- Class II
- Regulation Number
- 866.5870
- Review Panel
- IM
- Submission Type