510(k) K812188
K812188 is an FDA 510(k) premarket notification submitted by American Scientific Products for the device "CRYPTOCOCCAL ANTIGEN LATEX AGGLUTI". The FDA issued a decision of Substantially Equivalent on August 31, 1981. The device falls under product code GMD (Antisera, Latex Agglutination, Cryptococcus Neoformans), a Class II device regulated under 21 CFR 866.3165. American Scientific Products has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 31, 1981
- Date Received
- August 3, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antisera, Latex Agglutination, Cryptococcus Neoformans
- Device Class
- Class II
- Regulation Number
- 866.3165
- Review Panel
- MI
- Submission Type