510(k) K905544
K905544 is an FDA 510(k) premarket notification submitted by Amresco, Inc. for the device "MAGNESIUM REAGENT". The FDA issued a decision of Substantially Equivalent on December 27, 1990. The device falls under product code JGJ (Photometric Method, Magnesium), a Class I device regulated under 21 CFR 862.1495. Amresco, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 27, 1990
- Date Received
- December 11, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Photometric Method, Magnesium
- Device Class
- Class I
- Regulation Number
- 862.1495
- Review Panel
- CH
- Submission Type