510(k) K942192
K942192 is an FDA 510(k) premarket notification submitted by Sigma Diagnostics, Inc. for the device "THEOPHYLLINE FPIA REAGENT SET AND CALIBRATORS". The FDA issued a decision of Substantially Equivalent on July 13, 1994. The device falls under product code LER (Fluorescent Immunoassay, Theophylline), a Class II device regulated under 21 CFR 862.3880. Sigma Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 13, 1994
- Date Received
- May 4, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Fluorescent Immunoassay, Theophylline
- Device Class
- Class II
- Regulation Number
- 862.3880
- Review Panel
- TX
- Submission Type