510(k) K821318
K821318 is an FDA 510(k) premarket notification submitted by R&D Systems, Inc. for the device "RETIC SET". The FDA issued a decision of Substantially Equivalent on June 2, 1982. The device falls under product code KJN (Brilliant Cresyl Blue), a Class I device regulated under 21 CFR 864.1850. R&D Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 2, 1982
- Date Received
- May 4, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Brilliant Cresyl Blue
- Device Class
- Class I
- Regulation Number
- 864.1850
- Review Panel
- PA
- Submission Type