510(k) K931922
K931922 is an FDA 510(k) premarket notification submitted by Viratest Intl., Inc. for the device "DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT". The FDA issued a decision of Substantially Equivalent on March 30, 1994. The device falls under product code JSM (Culture Media, Non-Propagating Transport), a Class I device regulated under 21 CFR 866.2390. Viratest Intl., Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 30, 1994
- Date Received
- April 16, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Culture Media, Non-Propagating Transport
- Device Class
- Class I
- Regulation Number
- 866.2390
- Review Panel
- MI
- Submission Type