510(k) K990971
K990971 is an FDA 510(k) premarket notification submitted by Medica Corp. for the device "EASYLYTE QUALITY CONTROL KIT, MODELS 2814, 2815, 2816". The FDA issued a decision of Substantially Equivalent on April 27, 1999. The device falls under product code JJR (Electrolyte Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Medica Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 27, 1999
- Date Received
- March 23, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrolyte Controls (Assayed And Unassayed)
- Device Class
- Class I
- Regulation Number
- 862.1660
- Review Panel
- CH
- Submission Type