510(k) K842049
K842049 is an FDA 510(k) premarket notification submitted by Flow Laboratories, Inc. for the device "FLUOROSKAN". The FDA issued a decision of Substantially Equivalent on December 3, 1984. The device falls under product code JZT (Fluorometer), a Class I device regulated under 21 CFR 866.4520. Flow Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 3, 1984
- Date Received
- May 22, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Fluorometer
- Device Class
- Class I
- Regulation Number
- 866.4520
- Review Panel
- IM
- Submission Type