510(k) K890015
K890015 is an FDA 510(k) premarket notification submitted by Biotrol, USA, Inc. for the device "BIOTROL CHLORIDE". The FDA issued a decision of Substantially Equivalent on February 17, 1989. The device falls under product code CHJ (Mercuric Thiocyanate, Colorimetry, Chloride), a Class II device regulated under 21 CFR 862.1170. Biotrol, USA, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 17, 1989
- Date Received
- January 3, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mercuric Thiocyanate, Colorimetry, Chloride
- Device Class
- Class II
- Regulation Number
- 862.1170
- Review Panel
- CH
- Submission Type