510(k) K811671
K811671 is an FDA 510(k) premarket notification submitted by Zeus Scientific, Inc. for the device "CYTOMEGALOVIRUS ANTIBODY TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on September 16, 1981. The device falls under product code GQH (Antigen, Cf (Including Cf Control), Cytomegalovirus), a Class II device regulated under 21 CFR 866.3175. Zeus Scientific, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 16, 1981
- Date Received
- June 15, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antigen, Cf (Including Cf Control), Cytomegalovirus
- Device Class
- Class II
- Regulation Number
- 866.3175
- Review Panel
- MI
- Submission Type