510(k) K873530
K873530 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "PARAMAX MAGNESIUM REAGENT". The FDA issued a decision of Substantially Equivalent on Dec 14, 1987. The device falls under product code JGJ (Photometric Method, Magnesium), a Class I device regulated under 21 CFR 862.1495. Baxter Healthcare Corp has 507 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 14, 1987
- Date Received
- Sep 1, 1987
- 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
- 510(k)