510(k) K884192
K884192 is an FDA 510(k) premarket notification submitted by Baxter Diagnostics, Inc. for the device "RSV IFA TEST KIT FOR DIRECT ANTIGEN DETECTION". The FDA issued a decision of Substantially Equivalent on November 22, 1988. The device falls under product code LKT (Respiratory Syncytial Virus, Antigen, Antibody, Ifa), a Class I device regulated under 21 CFR 866.3480. Baxter Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 22, 1988
- Date Received
- October 6, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Respiratory Syncytial Virus, Antigen, Antibody, Ifa
- Device Class
- Class I
- Regulation Number
- 866.3480
- Review Panel
- MI
- Submission Type