510(k) K912838
K912838 is an FDA 510(k) premarket notification submitted by Baxter Diagnostics, Inc. for the device "BARTELS RESPIRATORY SYNCYTIAL VIRUS ENZYME IMMUNO". The FDA issued a decision of Substantially Equivalent on September 27, 1991. 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
- September 27, 1991
- Date Received
- June 26, 1991
- 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