510(k) K864206
K864206 is an FDA 510(k) premarket notification submitted by Wellcome Diagnostics for the device "REVEAL COLOUR STREP A ZL16". The FDA issued a decision of Substantially Equivalent on January 13, 1987. The device falls under product code GTZ (Antisera, All Groups, Streptococcus Spp.), a Class I device regulated under 21 CFR 866.3740. Wellcome Diagnostics has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 13, 1987
- Date Received
- October 27, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antisera, All Groups, Streptococcus Spp.
- Device Class
- Class I
- Regulation Number
- 866.3740
- Review Panel
- MI
- Submission Type