510(k) K890131
K890131 is an FDA 510(k) premarket notification submitted by V-Tech, Inc. for the device "TARGET(TM) QUANTITATIVE HCG". The FDA issued a decision of Substantially Equivalent on March 9, 1989. The device falls under product code JHI (Visual, Pregnancy Hcg, Prescription Use), a Class II device regulated under 21 CFR 862.1155. V-Tech, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 9, 1989
- Date Received
- January 12, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Visual, Pregnancy Hcg, Prescription Use
- Device Class
- Class II
- Regulation Number
- 862.1155
- Review Panel
- CH
- Submission Type