510(k) K800908
K800908 is an FDA 510(k) premarket notification submitted by Immuno-Mycologics, Inc. for the device "CAPIK-CANDIDA ALBICANS IDENT. KIT.". The FDA issued a decision of Substantially Equivalent on June 2, 1980. The device falls under product code JXB (Kit, Identification, Yeast), a Class I device regulated under 21 CFR 866.2660. Immuno-Mycologics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 2, 1980
- Date Received
- April 21, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Identification, Yeast
- Device Class
- Class I
- Regulation Number
- 866.2660
- Review Panel
- MI
- Submission Type