510(k) K932685
K932685 is an FDA 510(k) premarket notification submitted by Baxter Diagnostics, Inc. for the device "PARAMAX(R) THEOPHYLLINE REAGENT AND CALIBRATORS". The FDA issued a decision of Substantially Equivalent on September 24, 1993. The device falls under product code KLS (Enzyme Immunoassay, Theophylline), a Class II device regulated under 21 CFR 862.3880. Baxter Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 24, 1993
- Date Received
- June 3, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Immunoassay, Theophylline
- Device Class
- Class II
- Regulation Number
- 862.3880
- Review Panel
- TX
- Submission Type