510(k) K896420
K896420 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "DSL C-PEPTIDE RIA (DSL #7000)". The FDA issued a decision of Substantially Equivalent on May 24, 1990. The device falls under product code JKD (Radioimmunoassay, C-Peptides Of Proinsulin), a Class I device regulated under 21 CFR 862.1135. Diagnostic Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 24, 1990
- Date Received
- November 8, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, C-Peptides Of Proinsulin
- Device Class
- Class I
- Regulation Number
- 862.1135
- Review Panel
- CH
- Submission Type